Intergenerational Influence of Gender and the DM1 Phenotype of the Transmitting Parent in Korean Myotonic Dystrophy Type 1

Myotonic dystrophy type 1 (DM1) is the most common autosomal-dominant disorder caused by the CTG repeat expansion of the DMPK, and it has been categorized into three phenotypes: mild, classic, and congenital DM1. Here, we reviewed the intergenerational influence of gender and phenotype of the transm...

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Detalles Bibliográficos
Autores principales: Han, Ji Yoon, Jang, Woori, Park, Joonhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408469/
https://www.ncbi.nlm.nih.gov/pubmed/36011377
http://dx.doi.org/10.3390/genes13081465

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408469/
https://www.ncbi.nlm.nih.gov/pubmed/36011377
http://dx.doi.org/10.3390/genes13081465

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