Chart validation of an algorithm for identifying hereditary progressive muscular dystrophy in healthcare claims

BACKGROUND: Muscular dystrophies (MDs) are a group of inherited conditions characterized by progressive muscle degeneration and weakness. The rarity and heterogeneity of the population with MD have hindered therapeutic developments as well as epidemiological and health outcomes research. The objecti...

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Detalles Bibliográficos
Autores principales: Chen, Xiaoxue, Agiro, Abiy, Martin, Ann S., Lucas, Ann M., Haynes, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688201/
https://www.ncbi.nlm.nih.gov/pubmed/31399066
http://dx.doi.org/10.1186/s12874-019-0816-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688201/
https://www.ncbi.nlm.nih.gov/pubmed/31399066
http://dx.doi.org/10.1186/s12874-019-0816-7

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