Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity

Human Genetics

Volumn 103, Issue 4, 1998, Pages 455-461

  Raz, Tal ^a   Barrett, Tim ^b   Szargel, Raymonde ^a   Mandel, Hanna ^a   Neufeld, Ellis J ^c   Nosaka, Kazuto ^d   Viana, Marcos B ^e   Cohen, Nadine ^a  

^a TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^b UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^c BOSTON CHILDREN S HOSPITAL   (United States)

^d KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^e Department of Hematology   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

THIAMINE;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 1Q; CONTROLLED STUDY; DIABETES MELLITUS; DRUG MEGADOSE; ETHNIC GROUP; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; HUMAN; MAJOR CLINICAL STUDY; MALE; MEGALOBLASTIC ANEMIA; PERCEPTION DEAFNESS; PRIORITY JOURNAL; ROGERS SYNDROME;

ANEMIA, MEGALOBLASTIC; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; DEAFNESS; DIABETES MELLITUS; FEMALE; HAPLOTYPES; HUMANS; INFANT; LINKAGE DISEQUILIBRIUM; MALE; SYNDROME; THIAMINE;

EID: 0031752473     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050850     Document Type: Article

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