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Case Report: A Novel Missense Variant in the SIPA1L3 Gene Associated With Cataracts in a Chinese Family
The signal-induced proliferation-associated 1-like 3 (SIPA1L3) gene that encodes a putative Rap GTPase-activating protein (RapGAP) has been associated with congenital cataract and eye development abnormalities. However, our current understanding of the mutation spectrum of SIPA1L3 associated with ey...
Autores principales: | Yang, Duo, Zhou, Haiyan, Lin, Jiwu, Zhao, Shuangxi, Zhou, Hao, Yin, Zhaochu, Ni, Bin, Chen, Yong, Xie, Wanqin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481882/ https://www.ncbi.nlm.nih.gov/pubmed/34603379 http://dx.doi.org/10.3389/fgene.2021.715599 |
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