LAMA2‐related muscular dystrophy: Natural history of a large pediatric cohort

OBJECTIVE: To characterize natural history of Laminin‐α2 related muscular dystrophies (LAMA2‐RD) to help anticipating complications and identifying reliable outcome measures for clinical trial design and powering. METHODS: We conducted a retrospective, single‐center, cross‐sectional and longitudinal...

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Detalles Bibliográficos
Autores principales: Zambon, Alberto A., Ridout, Deborah, Main, Marion, Mein, Rachael, Phadke, Rahul, Muntoni, Francesco, Sarkozy, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545609/
https://www.ncbi.nlm.nih.gov/pubmed/32910545
http://dx.doi.org/10.1002/acn3.51172

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545609/
https://www.ncbi.nlm.nih.gov/pubmed/32910545
http://dx.doi.org/10.1002/acn3.51172

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