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A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signaling
Failure of neural tube closure during embryonic development can result in anencephaly, one of the most common birth defects in humans. A family with recurrent anencephalic fetuses was investigated to understand its etiology and pathogenesis. Exome sequencing revealed a recessive germline 21-bp in-fr...
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| Izdano u: | J Exp Med |
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| Glavni autori: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Rockefeller University Press
2020
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7953732/ https://ncbi.nlm.nih.gov/pubmed/32845958 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1084/jem.20191561 |
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