The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33

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Bibliographic Details
Published inAnnals of the New York Academy of Sciences Vol. 883; no. 1; pp. 453 - 456
Main Authors GUILBOT, A., KESSALI, M., RAVISÉ, N., HAMMADOUCHE, T., BOUHOUCHE, A., MAISONOBE, T., GRID, D., BRICE, A., LeGUERN, E.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.10.1999
Subjects
Algeria
Charcot-Marie-Tooth Disease - classification
Charcot-Marie-Tooth Disease - genetics
Chromosome Mapping
Chromosomes, Human, Pair 5
Consanguinity
Female
Genes, Recessive
Genetic Markers
Homozygote
Humans
Male
Algeria
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More Information
Bibliography:ark:/67375/WNG-84R8SXJ6-K
ArticleID:NYAS453
istex:15ECBD373B67E5121D86F599F7AED906E5A2015C
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0077-8923
1749-6632
DOI:10.1111/j.1749-6632.1999.tb08608.x