Asymptomatic Familial Hyperprolactinemia Caused by a Unique bi-Allelic Variant in the Prolactin-Receptor Gene

Yoav Natif, Matan M. Jean,Ohad S. Birk,Marina Eskin‐Schwartz,Merav Fraenkel, Uri Yoel

Endocrine Abstracts(2023)

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摘要
Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | ISSN 1479-6848 (online)
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gene,bi-allelic,prolactin-receptor
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