A novel homozygous mutation of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia.

Chin Med J (Engl)

Department of Endocrinology, The First Medical Center, Chinese PLA General Hospital, Beijing 100853, China.

Published: June 2021

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367063	PMC
http://dx.doi.org/10.1097/CM9.0000000000001568	DOI Listing

Publication Analysis

novel homozygous

homozygous mutation

mutation calcium-sensing

calcium-sensing receptor

receptor gene

gene associated

associated apparent

apparent autosomal

autosomal recessive

recessive inheritance

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