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A novel homozygous mutation of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia.
Li, Nan; Li, Xiang; Ni, Xiao-Lin; Li, Xiu-Ying; Xia, Wei-Bo; Yang, Guo-Qing; Pei, Yu.
Afiliação
  • Li N; Department of Endocrinology, The First Medical Center, Chinese PLA General Hospital, Beijing 100853, China.
  • Li X; Department of Endocrinology, The Second Medical Center, Chinese PLA General Hospital, Beijing 100853, China.
  • Ni XL; Department of Endocrinology, Key Laboratory of Endocrinology, Ministry of Health, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing 100730, China.
  • Li XY; Department of Endocrinology, Key Laboratory of Endocrinology, Ministry of Health, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing 100730, China.
  • Xia WB; Department of Endocrinology, The First Medical Center, Chinese PLA General Hospital, Beijing 100853, China.
  • Yang GQ; Department of Endocrinology, Liangxiang Teaching Hospital, Capital Medical University, Beijing 102401, China.
  • Pei Y; Department of Endocrinology, Key Laboratory of Endocrinology, Ministry of Health, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing 100730, China.
Chin Med J (Engl) ; 134(15): 1869-1871, 2021 06 15.
Article em En | MEDLINE | ID: mdl-34397587
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Detecção de Cálcio / Hipercalcemia Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Detecção de Cálcio / Hipercalcemia Idioma: En Ano de publicação: 2021 Tipo de documento: Article