Two novel mutations in the KHDC3L gene in Asian patients with recurrent hydatidiform mole

Recurrent hydatidiform mole (RHM) is defined by the occurrence of repeated molar pregnancies in affected women. Two genes, NLRP7 and KHDC3L, play a causal role in RHM and are responsible for 48–80% and 5% of cases, respectively. Here, we report the results of screening these two genes for mutations...

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Detalles Bibliográficos
Autores principales: Rezaei, Maryam, Nguyen, Ngoc Minh Phuong, Foroughinia, Leila, Dash, Pratima, Ahmadpour, Fatemeh, Verma, Ishwar Chandra, Slim, Rima, Fardaei, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007383/
https://www.ncbi.nlm.nih.gov/pubmed/27621838
http://dx.doi.org/10.1038/hgv.2016.27

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007383/
https://www.ncbi.nlm.nih.gov/pubmed/27621838
http://dx.doi.org/10.1038/hgv.2016.27

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