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Quoted phrase not found in phrase index: "Bethlem myopathy 1A"
Page 1
Natural history of pulmonary function in collagen VI-related myopathies.
Brain. 2013 Dec;136(Pt 12):3625-33. doi: 10.1093/brain/awt284. Epub 2013 Nov 22.
Brain. 2013.
PMID: 24271325
Free PMC article.
Patients with better functional abilities, in whom walking with/without assistance was achieved, were initially combined, containing both intermediate and Bethlem myopathy phenotypes in one group. However, one subset of patients demonstrated a continuous decline in …
Patients with better functional abilities, in whom walking with/without assistance was achieved, were initially combined, containing both in …
Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies.
Bovolenta M, Neri M, Martoni E, Urciuolo A, Sabatelli P, Fabris M, Grumati P, Mercuri E, Bertini E, Merlini L, Bonaldo P, Ferlini A, Gualandi F.
Bovolenta M, et al.
BMC Med Genet. 2010 Mar 19;11:44. doi: 10.1186/1471-2350-11-44.
BMC Med Genet. 2010.
PMID: 20302629
Free PMC article.
BACKGROUND: Molecular characterization of collagen-VI related myopathies currently relies on standard sequencing, which yields a detection rate approximating 75-79% in Ullrich congenital muscular dystrophy (UCMD) and 60-65% in Bethlem myopathy (BM) patients as PCR-b …
BACKGROUND: Molecular characterization of collagen-VI related myopathies currently relies on standard sequencing, which yields a detection r …
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