Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: Exclusion of candidate genes including EGR1

European Journal of Human Genetics

Volumn 7, Issue 8, 1999, Pages 849-859

  Guilbot, Angèle ^a   Ravisé, Nicole ^a   Bouhouche, Ahmed ^d   Coullin, Philippe ^b   Birouk, Nazha ^d   Maisonobe, Thierry ^a   Kuntzer, Thierry ^e   Vial, Christophe ^f   Grid, Djamel ^c   Brice, Alexis ^a   LeGuern, Eric ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b Lab de Cytogénétique   (France)

^c GÉNÉTHON   (France)

^d IBN SINA HOSPITAL   (Morocco)

^e LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^f HÔPITAL NEUROLOGIQUE   (France)

Author keywords

5q32 physical mapping; Autosomal recessive form; CDX1 gene; Charcot Marie Tooth disease; EGR1 gene

Indexed keywords

CONTIG; MICROSATELLITE DNA;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 5Q; CYTOGENETICS; DEMYELINATING NEUROPATHY; FAMILY STUDY; FEMALE; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC SCREENING; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SCHWANN CELL; SEQUENCE ANALYSIS;

EID: 18844482532     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200382     Document Type: Article

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