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Relationships of Motor Changes with Cognitive and Neuropsychiatric Features in FMR1 Male Carriers Affected with Fragile X-Associated Tremor/Ataxia Syndrome

The premutation expansion of the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene on the X chromosome has been linked to a range of clinical and subclinical features. Nearly half of men with FMR1 premutation develop a neurodegenerative disorder; Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)...

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Detalles Bibliográficos
Autores principales:	Hocking, Darren R., Loesch, Danuta Z., Stimpson, Paige, Tassone, Flora, Atkinson, Anna, Storey, Elsdon
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688438/ https://www.ncbi.nlm.nih.gov/pubmed/36421873 http://dx.doi.org/10.3390/brainsci12111549

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