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TBC1D20 mediates autophagy as a key regulator of autophagosome maturation
In humans, loss of TBC1D20 (TBC1 domain family, member 20) protein function causes Warburg Micro syndrome 4 (WARBM4), an autosomal recessive disorder characterized by congenital eye, brain, and genital abnormalities. TBC1D20-deficient mice exhibit ocular abnormalities and male infertility. TBC1D20 i...
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| Publicado no: | Autophagy |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5079675/ https://ncbi.nlm.nih.gov/pubmed/27487390 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15548627.2016.1199300 |
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