Literature DB >> 12707439

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

A Driss1, S Noguchi, R Amouri, M Kefi, T Sasaki, K Sugie, S Souilem, Y K Hayashi, N Shimizu, S Minoshima, J Kudoh, F Hentati, I Nishino.   

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.

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Year:  2003        PMID: 12707439     DOI: 10.1212/01.wnl.0000065886.82930.c5

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  1 in total

1.  Magnetic Resonance Imaging Findings in the Muscle Tissue of Patients with Limb Girdle Muscular Dystrophy Type 2I Harboring the Founder Mutation c.545A>G in the FKRP Gene.

Authors:  Zhiying Xie; Jiangxi Xiao; Yiming Zheng; Zhaoxia Wang; Yun Yuan
Journal:  Biomed Res Int       Date:  2018-05-29       Impact factor: 3.411

  1 in total

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