Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3

Gene

Volumn 198, Issue 2 JAN, 1997, Pages 313-321

  Lafrenière, Ronald G ^a,d   Kibar, Zoha ^a   Rochefort, Daniel L ^a   Han, Fei Yu ^a   Fon, Edward A ^a   Dubé, Marie Pierre ^a   Kang, Xiaolin ^b   Baird, Stephen ^b   Korneluk, Robert G ^b   Rommens, Johanna M ^c   Rouleau, Guy A ^a  

^a MONTREAL GENERAL HOSPITAL   (Canada)

^b CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^c HOSPITAL FOR SICK CHILDREN   (Canada)

^d Shire BioChem Inc   (Canada)

Author keywords

APECED Autoimmune polyglandular disease type 1; EPM1 Progressive myoclonus epilepsy type 1; SSCP

Indexed keywords

HISTONE H2A;

ARTICLE; CHROMOSOME 21Q; GENE; GENE ISOLATION; GENE MAPPING; GENE STRUCTURE; GENETIC MARKER; GENETIC POLYMORPHISM; HUMAN; INTRON; MOLECULAR CLONING; MYOCLONUS EPILEPSY; PRIORITY JOURNAL; PSEUDOGENE; SINGLE STRAND CONFORMATION POLYMORPHISM;

AMINO ACID SEQUENCE; BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 21; COSMIDS; DNA, COMPLEMENTARY; EXONS; GENE EXPRESSION; GENES; HUMANS; INTRONS; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RESTRICTION MAPPING;

EID: 0030725414     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0378-1119(97)00333-8     Document Type: Article

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