Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to...

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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 Valérie Delague, Corinne Bareil, Sylvie Tuffery, Patrice Bouvagnet, Eliane Chouery, Salam Koussa, Thierry Maisonobe, Jacques Loiselet, André Mégarbané, Mireille Claustres The American Journal of Human Genetics Volume 67, Issue 1, Pages 236-243 (July 2000) DOI: 10.1086/302980 Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Transcript of Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to...

Page 1: 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.

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 

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

The American Journal of Human Genetics Volume 67, Issue 1, Pages 236-243 (July 2000)

DOI: 10.1086/302980

Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Page 2: 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.

Figure 1

The American Journal of Human Genetics 2000 67, 236-243DOI: (10.1086/302980) Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Page 3: 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.

Figure 2

The American Journal of Human Genetics 2000 67, 236-243DOI: (10.1086/302980) Copyright © 2000 The American Society of Human Genetics Terms and Conditions