Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families

BACKGROUND: Intellectual disability (ID) is a heterogeneous group of neurodevelopmental disorders that is characterized by significant impairment in intellectual and adaptive functioning with onset during the developmental period. Whole‐exome sequencing (WES)‐based studies in the consanguineous fami...

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Detalles Bibliográficos
Autores principales: Moudi, Mahdiyeh, Vahidi Mehrjardi, Mohammad Yahya, Hozhabri, Hossein, Metanat, Zahra, Kalantar, Seyed Mehdi, Taheri, Mohsen, Ghasemi, Nasrin, Dehghani, Mohammadreza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842163/
https://www.ncbi.nlm.nih.gov/pubmed/35019165
http://dx.doi.org/10.1002/jcla.24241

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842163/
https://www.ncbi.nlm.nih.gov/pubmed/35019165
http://dx.doi.org/10.1002/jcla.24241

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