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Combined sequence and copy number analysis improves diagnosis of limb girdle and other myopathies

Abstract Objective Clinical and genetic heterogeneities make diagnosis of limb‐girdle muscular dystrophy (LGMD) and other overlapping disorders of muscle weakness complicated and expensive. We aimed to develop a comprehensive next generation sequence‐based multi‐gene panel (“The Lantern Focused Neur...

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Principais autores: Babi R. R. Nallamilli, Yinghong Pan, Lisa Sniderman King, Lakshmanan Jagannathan, Vinish Ramachander, Ann Lucas, Jan Markind, Raffaella Colzani, Madhuri Hegde
Formato: Artigo
Idioma:Inglês
Publicado: Wiley 2023-11-01
Series:Annals of Clinical and Translational Neurology
Acceso en liña:https://doi.org/10.1002/acn3.51896
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