Skeletal, cardiac, and respiratory muscle function and histopathology in the P448Lneo− mouse model of FKRP-deficient muscular dystrophy

BACKGROUND: Fukutin-related protein (FKRP) mutations are the most common cause of dystroglycanopathies known to cause both limb girdle and congenital muscular dystrophy. The P448Lneo− mouse model has a knock-in mutation in the FKRP gene and develops skeletal, respiratory, and cardiac muscle disease....

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Detalhes bibliográficos
Publicado no:Skelet Muscle
Main Authors: Yu, Qing, Morales, Melissa, Li, Ning, Fritz, Alexander G., Ruobing, Ren, Blaeser, Anthony, Francois, Ershia, Lu, Qi-Long, Nagaraju, Kanneboyina, Spurney, Christopher F.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2018
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5889611/
https://ncbi.nlm.nih.gov/pubmed/29625576
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13395-018-0158-x
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