Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes-Reference-Cited by-同舟云学术

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Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes

Published:2024-07 Issue:7 Volume:111 Page:1383-1404
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Heimdörfer David,Vorleuter Alexander,Eschlböck Alexander,Spathopoulou Angeliki,Suarez-Cubero Marta,Farhan Hesso,Reiterer Veronika,Spanjaard Melanie,Schaaf Christian P.,Huber Lukas A.,Kremser Leopold,Sarg Bettina,Edenhofer Frank,Geley Stephan,de Araujo Mariana E.G.,Huettenhofer Alexander^ORCID

Funder

Austrian Science Fund

Publisher

Elsevier BV

Reference127 articles.

1. Prader-Willi Syndrome and Schaaf-Yang Syndrome: Neurodevelopmental Diseases Intersecting at the MAGEL2 Gene;Fountain;Dis. Basel Switz.,2016

2. RNAs of the human chromosome 15q11-q13 imprinted region;Chamberlain;Wiley Interdiscip. Rev. RNA,2013

3. Approach to the Patient With Prader–Willi Syndrome;Höybye;J. Clin. Endocrinol. Metab.,2022

4. Prader-Willi syndrome;Cassidy;Genet. Med.,2012

5. A Review of Prader–Willi Syndrome;Szabadi;Endocrines,2022

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