Genotype phenotype relation analysis in autosomal recessive Charcot-Marie-Tooth disease in Tunisia

Acta Myologica

Volumn 20, Issue MAY, 2001, Pages 25-28

  Hentati, F ^a   Ben Othmane, K ^a   Barhoumi, C ^a   Amouri, R ^a   Ben Hamida, Ch ^a   Ben Hamida, M ^a  

^a Institut National de Neurologie Tunisia   (Tunisia)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CLINICAL ARTICLE; CONFERENCE PAPER; CONTROLLED STUDY; GENE LOCUS; GENETIC ANALYSIS; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN TISSUE; NERVE BIOPSY; NERVE CONDUCTION; PHENOTYPE; TUNISIA;

EID: 0034895945     PISSN: 11282460     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (11)

1. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie Tooth disease to chromosome 8q
2. Autosomal recessive forms of hereditary motor and sensory neuropathy
3. Fine localization of the CMT4A locus using a PAC contig and haplotype analysis
4. Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33
5. Physical and genetic mapping of the CMT4A. A locus and exclusion of PMP-2 as the defect in CMT4A
6. Autosomal recessive Charcot Marie Tooth disease: Clinical and genetic aspects
7. Gene mapping in gypsies identifies a novel demyelinating neuropathy on chromosome 8q24
8. Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplo-type sharing
9. A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3