Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

BACKGROUND: Autosomal recessive limb-girdle muscular dystrophies (LGMD2) include a number of disorders with heterogeneous etiology that cause predominantly weakness and wasting of the shoulder and pelvic girdle muscles. In this study, we determined the frequency of LGMD subtypes within a cohort of C...

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Bibliografische gegevens
Hoofdauteurs: Stehlíková, Kristýna, Skálová, Daniela, Zídková, Jana, Mrázová, Lenka, Vondráček, Petr, Mazanec, Radim, Voháňka, Stanislav, Haberlová, Jana, Hermanová, Markéta, Zámečník, Josef, Souček, Ondřej, Ošlejšková, Hana, Dvořáčková, Nina, Solařová, Pavla, Fajkusová, Lenka
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2014
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4145250/
https://ncbi.nlm.nih.gov/pubmed/25135358
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-014-0154-7
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