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A Premature Stop Codon in MYO18B is Associated with Severe Nemaline Myopathy with Cardiomyopathy

Background: Nemaline myopathies (NM) are rare and severe muscle diseases characterized by the presence of nemaline bodies (rods) in muscle fibers. Although ten genes have been implicated in the etiology of NM, an important number of patients remain without a molecular diagnosis. Objective: Here we d...

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Bibliografski detalji
Izdano u:J Neuromuscul Dis
Glavni autori: Malfatti, Edoardo, Böhm, Johann, Lacène, Emmanuelle, Beuvin, Maud, Guy Brochier, Romero, Norma B., Laporte, Jocelyn
Format: Artigo
Jezik:Inglês
Izdano: IOS Press 2015
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5240573/
https://ncbi.nlm.nih.gov/pubmed/27858739
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JND-150085
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