Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I

Neurology. 2003 Apr 22;60(8):1341-4. doi: 10.1212/01.wnl.0000065886.82930.c5.

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

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Chromosomes, Human, Pair 19 / genetics
  • Consanguinity
  • Cytoskeletal Proteins / metabolism
  • Dystroglycans
  • Genes, Recessive
  • Glycosylation
  • Humans
  • Laminin / deficiency
  • Laminin / metabolism
  • Membrane Glycoproteins / metabolism
  • Muscle, Skeletal / chemistry
  • Muscle, Skeletal / pathology
  • Muscular Dystrophies / blood
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophies / pathology
  • Mutation, Missense
  • Nerve Tissue Proteins / genetics
  • Pentosyltransferases
  • Point Mutation
  • Protein Processing, Post-Translational
  • Proteins
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tunisia

Substances

  • Cytoskeletal Proteins
  • DAG1 protein, human
  • Laminin
  • Membrane Glycoproteins
  • Nerve Tissue Proteins
  • Proteins
  • laminin alpha 2
  • Dystroglycans
  • FKRP protein, human
  • Pentosyltransferases