Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1477-9560
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
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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
- Klassifikation
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Medizin, Gesundheit
- Urheber
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Naz, Arshi
Biswas, Arijit
Khan, Tehmina Nafees
Goodeve, Anne
Ahmed, Nisar
Saqlain, Nazish
Ahmed, Shariq
Ujjan, Ikram Din
Shamsi, Tahir S.
Oldenburg, Johannes
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s12959-019-0193-9
- URN
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urn:nbn:de:101:1-2019042420353569946625
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:58 MESZ
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Beteiligte
- 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
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