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Mirror syndromes regarding AKT3 mutations: Loss of function variant leading to microcephaly
Author(s) -
Ciaccio Claudia,
Cellini Elena,
Guerrini Renzo,
Pantaleoni Chiara,
Masson Riccardo
Publication year - 2020
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.61821
Subject(s) - microcephaly , function (biology) , computer science , content (measure theory) , loss function , mutation , data sharing , computational biology , genetics , biology , medicine , gene , phenotype , mathematical analysis , mathematics , alternative medicine , pathology