The autosomal recessive form of CMT disease linked to 5q31-q33

Annals of the New York Academy of Sciences

Volumn 883, Issue , 1999, Pages 56-59

  Guilbot, A ^a   Kessali, M ^b   Ravise N ^a   Hammadouche, T ^a,c   Bouhouche, A ^a,d   Maisonobe, T ^a   Grid, D ^b   Brice, A ^a   Leguern, E ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b CHU Mustapha   (Algeria)

^c Institut Pasteur d'Algerie   (Algeria)

^d IBN SINA HOSPITAL   (Morocco)

Author keywords

[No Author keywords available]

Indexed keywords

ALGERIA; ARTICLE; CASE REPORT; CHROMOSOME 5; CHROMOSOME MAP; CONSANGUINITY; FEMALE; GENETIC LINKAGE; GENETIC MARKER; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; RECESSIVE GENE;

ALGERIA; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 5; CONSANGUINITY; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; HUMANS; LINKAGE (GENETICS); MALE;

EID: 0033554352     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1999.tb08567.x     Document Type: Article

References (11)

1. BEN OTHMANE, K. et al. 1993. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Hum. Mol. Genet. 10: 1625-1628.
2. BEN OTHMANE, K. et al. 1995. Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A. Genomics 28: 286-290.
3. BOLINO, A. et al. 1996, Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheats to chromosome 11q23 by homozygosity mapping and haplotype sharing. Hum. Mol. Genet. 7: 1051-1054.
4. LEGUERN, E. et al. 1996. Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33. Hum. Mol. Genet. 10: 1685-1688.
5. KALAYDJIEVA, L. et al. 1996. Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24. Nat. Genet. 14: 214-217.
6. SALTMAN, D.L. et al. 1993. A physical map of 15 loci on human chromosome 5q23-q33 by two-color fluorescence in situ hybridization. Genomics 16: 726-732.
7. Li, X. et al. 1994. A YAC contig of approximately 3 Mb from human chromosome 5q31 ->q33.Genomics 3: 470-477.
8. DIB, C. et al. 1996. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 14: 152-154.
9. MALLO, G. et al. 1997. Molecular cloning, sequencing and expression of the mRNA encoding human Cdx1 and Cdx2 homeobox. Int. J. Cancer 74: 35-44.
10. GABREËLS-FESTEN, A., et al. 1999. Study on the gene and phenotypic characterization of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33. J. Neurol. Neurosurg. Psychiatry 66: 569-574.
11. SUBRAMANIAN, V. et al 1995. Disruption of the murine homeobox gene Cdx1 affects axial skeletal identities by altering the mesodermal expression domains of Hox genes. Cell 17: 641-653.