Other limb-girdle muscular dystrophies
Author:
Publisher
Elsevier
Reference46 articles.
1. An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker–Warburg syndrome (WWS) caused by a mutation in the POMT1 gene;Balci;Neuromuscul Disord,2005
2. Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker–Warburg syndrome;Beltran-Valero de Bernabe;Am J Hum Genet,2002
3. The titin–telethonin complex is a directed, superstable molecular bond in the muscle Z-disk;Bertz;Proc Natl Acad Sci U S A,2009
4. POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes;Biancheri;Biochem Biophys Res Commun,2007
5. Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I;Boito;Arch Neurol,2005
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1. Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in FKRP Gene;Child Neurology Open;2022-01
2. A novel noncoding FKRP mutation in early onset limb-girdle muscular dystrophy;Neurology Genetics;2019-12-26
3. Disparities in Health Care Utilization by Race Among Teenagers and Young Adults With Muscular Dystrophy;Medical Care;2014-10
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