Phenotype and Genotype Study of Chinese POMT2-Related α-Dystroglycanopathy
ObjectiveAlpha-dystroglycanopathy (α-DGP) is a subtype of muscular dystrophy caused by defects in the posttranslational glycosylation of α-dystroglycan (α-DG). Our study aimed to summarize the clinical and genetic features of POMT2-related α-DGP in a cohort of patients in China.MethodsPedigrees, cli...
Gardado en:
| Principais autores: | , , , , , , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Frontiers Media S.A.
2021-08-01
|
| Series: | Frontiers in Genetics |
| Assuntos: | |
| Acceso en liña: | https://www.frontiersin.org/articles/10.3389/fgene.2021.692479/full |
| Tags: |
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|