A Homozygous Splicing Mutation in PDE2A...

Movement Disorders 2020 / 03

A Homozygous Splicing Mutation in PDE2A in a Family with Atypical Rett Syndrome

Haidar, Zahraa, Jalkh, Nadine, Corbani, Sandra, Abou-Ghoch, Joelle, Fawaz, Ali, Mehawej, Cybel, Chouery, Eliane
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Language:
english
Journal:
Movement Disorders
DOI:
10.1002/mds.28023
Date:
March, 2020
File:
PDF, 617 KB
english, 2020
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