Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1477-9560

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population ; volume:17 ; number:1 ; day:4 ; month:4 ; year:2019 ; pages:1-3 ; date:12.2019
Thrombosis journal ; 17, Heft 1 (4.4.2019), 1-3, 12.2019

Classification: Medizin, Gesundheit

Creator: Naz, Arshi
Biswas, Arijit
Khan, Tehmina Nafees
Goodeve, Anne
Ahmed, Nisar
Saqlain, Nazish
Ahmed, Shariq
Ujjan, Ikram Din
Shamsi, Tahir S.
Oldenburg, Johannes

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12959-019-0193-9

URN: urn:nbn:de:101:1-2019042420353569946625

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:58 AM CEST

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Associated

Naz, Arshi
Biswas, Arijit
Khan, Tehmina Nafees
Goodeve, Anne
Ahmed, Nisar
Saqlain, Nazish
Ahmed, Shariq
Ujjan, Ikram Din
Shamsi, Tahir S.
Oldenburg, Johannes
SpringerLink (Online service)

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Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect

Missense mutations in the CITED2 gene may contribute to congenital heart disease

Distinct functional consequences of ECEL1/DINE missense mutations in the pathogenesis of congenital contracture disorders

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Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

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Role of SMAD4 missense mutations in colorectal cancer progression

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MutaCYP: Classification of missense mutations in human cytochromes P450

Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect

Missense mutations in the CITED2 gene may contribute to congenital heart disease

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Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

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Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia

MutaCYP: Classification of missense mutations in human cytochromes P450

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Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

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Other Objects (12)

Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect

Missense mutations in the CITED2 gene may contribute to congenital heart disease

Distinct functional consequences of ECEL1/DINE missense mutations in the pathogenesis of congenital contracture disorders

Functional analysis of disease-associated CASK missense mutations

Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

Role of SMAD4 missense mutations in colorectal cancer progression

Identification of Pathogenic Missense Mutations of NF1 Using Computational Approaches

Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients

Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia

MutaCYP: Classification of missense mutations in human cytochromes P450

Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect

Missense mutations in the CITED2 gene may contribute to congenital heart disease

Distinct functional consequences of ECEL1/DINE missense mutations in the pathogenesis of congenital contracture disorders

Functional analysis of disease-associated CASK missense mutations

Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

Role of SMAD4 missense mutations in colorectal cancer progression

Identification of Pathogenic Missense Mutations of NF1 Using Computational Approaches

Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients

Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia

MutaCYP: Classification of missense mutations in human cytochromes P450

Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect

Missense mutations in the CITED2 gene may contribute to congenital heart disease

Distinct functional consequences of ECEL1/DINE missense mutations in the pathogenesis of congenital contracture disorders

Functional analysis of disease-associated CASK missense mutations

Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

Role of SMAD4 missense mutations in colorectal cancer progression

Identification of Pathogenic Missense Mutations of NF1 Using Computational Approaches

Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients

Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia

MutaCYP: Classification of missense mutations in human cytochromes P450

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