FMR1 gene CGG repeat distribution among the three individual cohorts with intellectual disability, autism, and primary ovarian insufficiency from Tamil Nadu, Southern India

Fragile X syndrome is the most common genetic cause of intellectual disability (ID) and is also well known to have a role in primary ovarian insufficiency (POI) and fragile X‐associated tremor ataxia syndrome (FXTAS) that expresses across generations. The objective was to compare the CGG repeat vari...

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Detalles Bibliográficos
Autores principales: Nagarathinam, Indhumathi, Chong, Samuel S., B. K., Thelma, Justin Margret, Jeffrey, Venkataraman, Viswanathan, Natarajan Padmavathy, Karthikeyen, Srisailapathy, C. R. Srikumari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744524/
https://www.ncbi.nlm.nih.gov/pubmed/36618123
http://dx.doi.org/10.1002/ggn2.10048

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744524/
https://www.ncbi.nlm.nih.gov/pubmed/36618123
http://dx.doi.org/10.1002/ggn2.10048

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