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Clinical, Molecular, and Computational Analysis in Patients With a Novel Double Mutation and a New Synonymous Variant in MeCP2: Report of the First Missense Mutation Within the AT-hook1 Cluster in Rett Syndrome
Kharrat, Marwa, Kamoun, Yosra, Kamoun, Fatma, Ellouze, Emna, Maalej, Marwa, Fendri-Kriaa, Nourhene, Ammar-Keskes, Leila, Belghith, Neila, Gargouri, Ali, Triki, Chahnez, Fakhfakh, FaizaLanguage:
english
Journal:
Journal of Child Neurology
DOI:
10.1177/0883073817701622
Date:
April, 2017
File:
PDF, 609 KB
english, 2017