Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing

Human Molecular Genetics

Volumn 5, Issue 7, 1996, Pages 1051-1054

  Bolino, Alessandra ^a   Brancolini, Valeria ^b   Bono, Francesco ^c   Bruni, Amalia ^d   Gambardella, Antonio ^c   Romeo, Giovanni ^a   Quattrone, Aldo ^c   Devoto, Marcella ^a,b  

^a G GASLINI INSTITUTE   (Italy)

^b Och Spine at New York Presbyterian Hospitals   (United States)

^c Facolta di Medicina   (Italy)

^d CNR USL6   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 11Q; CLINICAL ARTICLE; DEMYELINATING NEUROPATHY; FEMALE; GENE LOCATION; GENE MAPPING; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; MALE; MYELIN SHEATH; PRIORITY JOURNAL;

CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CONSANGUINITY; FEMALE; GENES, RECESSIVE; HAPLOTYPES; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE;

EID: 0030015647     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.7.1051     Document Type: Article

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