A Ca2+-sensing receptor mutation causes hypoparathyroidism by increasing receptor sensitivity to Ca2+ and maximal signal transduction

Pediatric Research

Volumn 42, Issue 4, 1997, Pages 443-447

  Mancilla, Edna E ^a   De Luca, Francesco ^a   Ray, Kausik ^b   Winer, Karen K ^a   Fan, Gao Feng ^b   Baron, Jeffrey ^a  

^a EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

^b NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; VITAMIN D DERIVATIVE;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; FEMALE; HETEROZYGOSITY; HUMAN; HYPERCALCIURIA; HYPOPARATHYROIDISM; KIDNEY CALCIFICATION; KIDNEY FAILURE; MISSENSE MUTATION; MUSCLE SPASM; PRIORITY JOURNAL; SEIZURE; SIGNAL TRANSDUCTION; SITE DIRECTED MUTAGENESIS;

EID: 0030861968     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/00006450-199710000-00004     Document Type: Article

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