Whole‐exome sequencing identifies a homozygous donor splice‐site mutation in STAG3 that causes primary ovarian insufficiency

Publisher： John Wiley & Sons Inc

E-ISSN： 1399-0004|93|2|340-344

ISSN： 0009-9163

Source： CLINICAL GENETICS, Vol.93, Iss.2, 2018-02, pp. : 340-344

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