Case Report: A Boy From a Consanguineous Family Diagnosed With Congenital Muscular Dystrophy Caused by Integrin Alpha 7 (ITGA7) Mutation

Introduction: Congenital muscular dystrophy (CMD) is a group of early-onset disorders with clinical and genetic heterogeneity. Patients always present with muscle weakness typically from birth to early infancy, delay or arrest of gross motor development, and joint and/or spinal rigidity. There are v...

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Detalles Bibliográficos
Autores principales: Xia, Wenqing, Ni, Zhumei, Zhang, Zheng, Sang, Hongfei, Liu, Huifang, Chen, Zhenzhen, Jiang, Lin, Yin, Congguo, Huang, Jinyu, Li, Lingfei, Lei, Xiaoguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450528/
https://www.ncbi.nlm.nih.gov/pubmed/34552617
http://dx.doi.org/10.3389/fgene.2021.706823

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450528/
https://www.ncbi.nlm.nih.gov/pubmed/34552617
http://dx.doi.org/10.3389/fgene.2021.706823

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