Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene ; volume:74 ; number:2 ; day:1 ; month:6 ; year:2024 ; pages:1 ; date:6.2024
Journal of molecular neuroscience ; 74, Heft 2 (1.6.2024), 1, 6.2024

Creator: Elaraby, Nesma M.
Ahmed, Hoda A.
Ashaat, Neveen A.
Tawfik, Sameh
Ahmed, Mahmoud K. H.
Hassib, Nehal F.
Ashaat, Engy A.

Contributor: SpringerLink (Online service)

DOI: 10.1007/s12031-024-02233-3

URN: urn:nbn:de:101:1-2410052135457.915945906724

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

Last update: 15.08.2025, 7:19 AM CEST

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Elaraby, Nesma M.
Ahmed, Hoda A.
Ashaat, Neveen A.
Tawfik, Sameh
Ahmed, Mahmoud K. H.
Hassib, Nehal F.
Ashaat, Engy A.
SpringerLink (Online service)

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Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene

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Other Objects (12)

Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature

A novel variant of DNM1L expanding the clinical phenotypic spectrum: a case report and literature review

Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum

Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders

EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum

Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II

Insights into the expanding intestinal phenotypic spectrum of SOCS1 haploinsufficiency and therapeutic options

Expanding the genotypic and phenotypic spectrum of Egyptian children with maple syrup urine disease

Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancy

Expanding the phenotypic and genetic spectrum of GTPBP3 deficiency: findings from nine Chinese pedigrees

Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males

AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant

Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature

A novel variant of DNM1L expanding the clinical phenotypic spectrum: a case report and literature review

Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum

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EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum

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Insights into the expanding intestinal phenotypic spectrum of SOCS1 haploinsufficiency and therapeutic options

Expanding the genotypic and phenotypic spectrum of Egyptian children with maple syrup urine disease

Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancy

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