The Role of AKT3 Copy Number Changes in Brain Abnormalities and Neurodevelopmental Disorders: Four New Cases and Literature Review

Microdeletions at 1q43-q44 have been described as resulting in a clinically recognizable phenotype of intellectual disability (ID), facial dysmorphisms and microcephaly (MIC). In contrast, the reciprocal microduplications of 1q43-q44 region have been less frequently reported and patients showed a va...

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Detalles Bibliográficos
Autores principales: Lopes, Fátima, Torres, Fátima, Soares, Gabriela, van Karnebeek, Clara D., Martins, Cecília, Antunes, Diana, Silva, João, Muttucomaroe, Lauren, Botelho, Luís Filipe, Sousa, Susana, Rendeiro, Paula, Tavares, Purificação, Van Esch, Hilde, Rajcan-Separovic, Evica, Maciel, Patrícia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395382/
https://www.ncbi.nlm.nih.gov/pubmed/30853971
http://dx.doi.org/10.3389/fgene.2019.00058

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395382/
https://www.ncbi.nlm.nih.gov/pubmed/30853971
http://dx.doi.org/10.3389/fgene.2019.00058

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