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MON-539 Mice Harboring a Germline Heterozygous AP2S1 Mutation, Arg15Leu, Are a Model for Familial Hypocalciuric Hypercalcemia Type 3 (FHH3)
Author(s) -
Fadil Hannan,
Victoria Stokes,
Caroline M. Gorvin,
Tertius Hough,
Gemma Codner,
Michelle Stewart,
Sara Wells,
Lydia Teboul,
Rajesh Thakker
Publication year - 2019
Publication title -
journal of the endocrine society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.046
H-Index - 20
ISSN - 2472-1972
DOI - 10.1210/js.2019-mon-539
Subject(s) - germline , germline mutation , genetics , medicine , mutation , endocrinology , biology , gene

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