Diagnostically important muscle pathology in DNAJB6 mutated LGMD1D

INTRODUCTION: Limb girdle muscular dystrophies are a large group of both dominantly and recessively inherited muscle diseases. LGMD1D is caused by mutated DNAJB6 and the molecular pathogenesis is mediated by defective chaperonal function leading to impaired handling of misfolded proteins which norma...

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Detalles Bibliográficos
Autores principales: Sandell, Satu, Huovinen, Sanna, Palmio, Johanna, Raheem, Olayinka, Lindfors, Mikaela, Zhao, Fang, Haapasalo, Hannu, Udd, Bjarne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743201/
https://www.ncbi.nlm.nih.gov/pubmed/26847086
http://dx.doi.org/10.1186/s40478-016-0276-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743201/
https://www.ncbi.nlm.nih.gov/pubmed/26847086
http://dx.doi.org/10.1186/s40478-016-0276-9

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