Hereditary defects in vitamin d-deficiency rickets;Étiologie moléculaire des rachitismes vitamino-dépendants héréditaires

Medecine/Sciences

Volumn 17, Issue 12, 2001, Pages 1289-1296

  Saint Arnaud, R ^a   Dardenne, O ^a   Glorieux, F H ^a  

^a SHRINERS HOSPITAL FOR CHILDREN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIDIOL 1 MONOOXYGENASE; CYTOCHROME P450; VITAMIN D; VITAMIN D RECEPTOR;

DELETION MUTANT; GENE DUPLICATION; GENE EXPRESSION REGULATION; GENETIC DISORDER; HUMAN; MISSENSE MUTATION; NONHUMAN; NONSENSE MUTATION; PHENOTYPE; REVIEW; VITAMIN D DEFICIENCY; VITAMIN D METABOLISM; VITAMIN D RESISTANT RICKETS;

ANIMALIA;

EID: 17644439223     PISSN: 07670974     EISSN: None     Source Type: Journal    
DOI: 10.1051/medsci/200117121289     Document Type: Review

References (38)

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