Cloning of human 25-hydroxyvitamin D-1α-hydroxylase and mutations causing vitamin D-dependent rickets type 1

Molecular Endocrinology

Volumn 11, Issue 13, 1997, Pages 1961-1970

  Fu, Glenn K ^a   Lin, Dong ^a   Zhang, Martin Y H ^a   Bikle, Daniel D ^a,b   Shackleton, Cedric H L ^c   Miller, Walter L ^a   Portale, Anthony A ^a,d  

^a Child Health Research Center   (United States)

^b SAN FRANCISCO VETERANS AFFAIRS MEDICAL CENTER   (United States)

^c CHILDREN S HOSPITAL OAKLAND RESEARCH INSTITUTE   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIDIOL 1 MONOOXYGENASE;

ARTICLE; BRAIN; CASE REPORT; CHROMOSOME 12; DELETION MUTANT; DNA SEQUENCE; ENZYME DEFICIENCY; FEMALE; FRAMESHIFT MUTATION; GENE EXPRESSION; GENE LOCATION; GENE MUTATION; HUMAN; HUMAN CELL; INFANT; KIDNEY; MOLECULAR CLONING; PRIORITY JOURNAL; RICKETS; RNA ANALYSIS; TESTIS; TISSUE DISTRIBUTION;

MAMMALIA;

EID: 0030782757     PISSN: 08888809     EISSN: None     Source Type: Journal    
DOI: 10.1210/mend.11.13.0035     Document Type: Article

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