A novel de novo RNF216 mutation associated with autosomal recessive Huntington‐like disorder

Mutations in RNF216 have been found to be associated with autosomal recessive Huntington‐like disorder. Here, we describe a patient with Huntington‐like disorder caused by a novel de novo RNF216 mutation. The patient started to have choreatic movements of both hands, slowly progressing to head, face...

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Detalles Bibliográficos
Autores principales: Chen, Ke‐Liang, Zhao, Gui‐Xian, Wang, He, Wei, Lei, Huang, Yu‐Yuan, Chen, Shi‐Dong, Lin, Bi‐Ying, Dong, Qiang, Cui, Mei, Yu, Jin‐Tai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261743/
https://www.ncbi.nlm.nih.gov/pubmed/32358900
http://dx.doi.org/10.1002/acn3.51047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261743/
https://www.ncbi.nlm.nih.gov/pubmed/32358900
http://dx.doi.org/10.1002/acn3.51047

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