High prevalence and phenotypeâgenotype correlations of limb girdle muscular dystrophy type 2I in Denmark
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference32 articles.
1. Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C;Brockington;Hum Mol Genet,2001
2. Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin α2 deficiency and abnormal glycosylation of α-dystroglycan;Brockington;Am J Hum Genet,2001
3. A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3;Driss;Neuromusc Disord,2000
4. Journey into muscular dystrophies caused by abnormal glycosylation;Muntoni;Acta Myol,2004
5. A role for dystroglycan in basement membrane assembly;Henry;Cell,1998
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