Abstract
The authors mapped an autosomal recessive form of limb-girdle MD on chromosome 19q13.3 (LGMD2I), further narrowed down the candidate region to 1.1 Mb, and identified one new homozygous mutation in the fukutin-related protein (FKRP) gene on patients of the original Tunisian family. Immunohistochemical and immunoblot analysis showed abnormal expression of alpha-dystroglycan and laminin-alpha2 supporting the hypothesis that FKRP has a role in the interaction between the extracellular matrix components.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Substitution
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Chromosomes, Human, Pair 19 / genetics
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Consanguinity
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Cytoskeletal Proteins / metabolism
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Dystroglycans
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Genes, Recessive
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Glycosylation
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Humans
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Laminin / deficiency
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Laminin / metabolism
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Membrane Glycoproteins / metabolism
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Muscle, Skeletal / chemistry
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Muscle, Skeletal / pathology
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Muscular Dystrophies / blood
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Muscular Dystrophies / genetics*
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Muscular Dystrophies / pathology
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Mutation, Missense
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Nerve Tissue Proteins / genetics
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Pentosyltransferases
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Point Mutation
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Protein Processing, Post-Translational
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Proteins
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Reverse Transcriptase Polymerase Chain Reaction
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Tunisia
Substances
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Cytoskeletal Proteins
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DAG1 protein, human
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Laminin
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Membrane Glycoproteins
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Nerve Tissue Proteins
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Proteins
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laminin alpha 2
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Dystroglycans
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FKRP protein, human
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Pentosyltransferases