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A Homozygous Splicing Mutation in PDE2A in a Family With Atypical Rett Syndrome
Author(s) -
Haidar Zahraa,
Jalkh Nadine,
Corbani Sandra,
AbouGhoch Joelle,
Fawaz Ali,
Mehawej Cybel,
Chouery Eliane
Publication year - 2020
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.28023
Subject(s) - medical genetics , unit (ring theory) , saint , medicine , genetics , biology , psychology , history , art history , mathematics education , gene
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