Gonadal mosaicism in GNAO1 causing neurodevelopmental disorder with involuntary movements; two additional variants
Background: GNAO1 encodes an alpha subunit of the heterotrimeric guanine nucleotide-binding proteins (G proteins). Mutations in GNAO1 result in two clinical phenotypes: Early infantile epileptic encephalopathy 17 (EEIE17-OMIM #615473) and Neurodevelopmental disorder with involuntary movements (NEDIM...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2022-06-01
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Series: | Molecular Genetics and Metabolism Reports |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2214426922000246 |