Identification of a new locus for autosomal recessive Charcot-Marie- Tooth disease with focally folded myelin on chromosome 11p15

Genomics

Volumn 62, Issue 3, 1999, Pages 344-349

  Ben Othmane, Kamel ^a   Johnson, Ellen ^a   Menold, Marisa ^a   Graham, Felicia L ^a   Ben Hamida, Mongi ^b   Hasegawa, Osamu ^c   Rogala, Allison D ^a   Ohnishi, Akio ^d   Pericak Vance, Margaret ^a   Hentati, Faycal ^b   Vance, Jeffery M ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b Institut National de Neurologie Tunisia   (Tunisia)

^c YOKOHAMA CITY UNIVERSITY   (Japan)

^d UNIVERSITY OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 11P; CLINICAL ARTICLE; DEMYELINATING DISEASE; GENE MAPPING; GENETIC LINKAGE; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MYELIN SHEATH; NEUROPATHY; PEDIGREE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL;

EID: 17344376225     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.6028     Document Type: Article

References (25)

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