A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus-Reference-Cited by-同舟云学术

A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus

Published:1998-07 Issue:1 Volume:63 Page:140-147
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Weiler Tracey,Greenberg Cheryl R.,Zelinski Teresa,Nylen Edward,Coghlan Gail,Crumley M. Joyce,Fujiwara T. Mary,Morgan Kenneth,Wrogemann Klaus

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference50 articles.

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2. Automatic selection of loop breakers for genetic linkage analysis;Becker;Hum Hered,1998

3. β-Sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex;Bönnemann;Nat Genet,1995

4. Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E);Bönnemann;Hum Mol Genet,1996

5. Diagnostic criteria for the limb-girdle muscular dystrophies: report of the ENMC consortium on limb-girdle dystrophies;Bushby;Neuromusc Disord,1995

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