LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials

OBJECTIVE: To delineate the full phenotypic spectrum and characterize the natural history of limb girdle muscular dystrophy type D1 (LGMDD1). METHODS: We extracted age at clinical events of interest contributing to LGMDD1 disease burden via a systematic literature and chart review. Manual muscle tes...

Descripción completa

Detalles Bibliográficos
Autores principales: Findlay, Andrew R., Robinson, Sarah E., Poelker, Stephanie, Seiffert, Michelle, Bengoechea, Rocio, Weihl, Conrad C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930420/
https://www.ncbi.nlm.nih.gov/pubmed/36427278
http://dx.doi.org/10.1002/acn3.51709

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930420/
https://www.ncbi.nlm.nih.gov/pubmed/36427278
http://dx.doi.org/10.1002/acn3.51709

Ejemplares similares