Heterozygous ZNHIT3 variants within the 17q12 recurrent deletion region are associated with Mayer-Rokitansky-Kuster Hauser (MRKH) syndrome
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Published:2024-08
Issue:
Volume:589
Page:112237
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ISSN:0303-7207
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Container-title:Molecular and Cellular Endocrinology
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language:en
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Short-container-title:Molecular and Cellular Endocrinology
Author:
Brakta SoumiaORCID,
Du QuanshengORCID,
Chorich Lynn P.,
Hawkins Zoe A.,
Sullivan Megan E.,
Ko Eun Kyung,
Kim Hyung-Goo,
Knight JamesORCID,
Taylor Hugh S.,
Friez Michael,
Phillips John A.,
Layman Lawrence C.