Prenatal muscle development in a mouse model for the secondary dystroglycanopathies

BACKGROUND: The defective glycosylation of α-dystroglycan is associated with a group of muscular dystrophies that are collectively referred to as the secondary dystroglycanopathies. Mutations in the gene encoding fukutin-related protein (FKRP) are one of the most common causes of secondary dystrogly...

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Detalles Bibliográficos
Autores principales: Kim, Jihee, Hopkinson, Mark, Kavishwar, Manoli, Fernandez-Fuente, Marta, Brown, Susan Carol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759920/
https://www.ncbi.nlm.nih.gov/pubmed/26900448
http://dx.doi.org/10.1186/s13395-016-0073-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759920/
https://www.ncbi.nlm.nih.gov/pubmed/26900448
http://dx.doi.org/10.1186/s13395-016-0073-y

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