Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles

Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles

Background: Recurrent hydatidiform moles (RHMs) are an unusual pregnancy with at least two molar gestations that are associated with abnormal proliferation of trophoblastic tissue and a failure in the embryonic tissues development. Three maternal-effect genes, including NLRP7, KHDC3L, and PADI6 have...

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Bibliographic Details
Main Authors: Jafar Fallahi, Zahra Anvar, Vahid Razban, Mozhdeh Momtahan, Bahia Namavar-Jahromi, Majid Fardaei
Format: Article
Language:English
Published: Shiraz University of Medical Sciences 2020-03-01
Series:Iranian Journal of Medical Sciences
Subjects:
haplotypes
khdc3l protein, human
hydatidiform mole
founder effect
mutatio
Online Access:http://ijms.sums.ac.ir/article_45335_ff97851293beac95f30505b2ee760138.pdf

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