Mirror syndromes regarding <scp>AKT3</scp> mutations: Loss of function variant leading to microcephaly

Authors :: Riccardo Masson
Claudia Ciaccio
Elena Cellini
Renzo Guerrini
Chiara Pantaleoni
Source :: American Journal of Medical Genetics Part A. 182:2800-2802
Publication Year :: 2020
Publisher :: Wiley, 2020.

Subjects :: Microcephaly
Text mining
business.industry
Genetics
MEDLINE
medicine
Biology
business
medicine.disease
Bioinformatics
Genetics (clinical)
Loss function
AKT3

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