Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I

BACKGROUND: Limb girdle muscular dystrophies (LGMD) are inclusive of 7 autosomal dominant and 14 autosomal recessive disorders featuring progressive muscle weakness and atrophy. Studies of cardiac function have not yet been well-defined in deficiencies of dysferlin (LGMD2B) and fukutin related prote...

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Detalles Bibliográficos
Autores principales: Rosales, Xiomara Q, Moser, Sean J, Tran, Tam, McCarthy, Beth, Dunn, Nicholas, Habib, Philip, Simonetti, Orlando P, Mendell, Jerry R, Raman, Subha V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170213/
https://www.ncbi.nlm.nih.gov/pubmed/21816046
http://dx.doi.org/10.1186/1532-429X-13-39

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170213/
https://www.ncbi.nlm.nih.gov/pubmed/21816046
http://dx.doi.org/10.1186/1532-429X-13-39

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