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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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| Publicado no: | Hum Genome Var |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5007383/ https://ncbi.nlm.nih.gov/pubmed/27621838 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2016.27 |
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