Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to 19q13.1-13.3 in a Large Consanguineous Lebanese Family: Exclusion of MAG as a Candidate Gene-Reference-Cited by-同舟云学术

Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to 19q13.1-13.3 in a Large Consanguineous Lebanese Family: Exclusion of MAG as a Candidate Gene

Published:2000-07 Issue:1 Volume:67 Page:236-243
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Delague Valérie,Bareil Corinne,Tuffery Sylvie,Bouvagnet Patrice,Chouery Eliane,Koussa Salam,Maisonobe Thierry,Loiselet Jacques,Mégarbané André,Claustres Mireille

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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4. Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15;Ben Othmane;Genomics,1999

5. Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing;Bolino;Hum Mol Genet,1996

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