Preliminary report on screening IGSF3 gene mutation in families with congenital absence of lacrimal puncta and canaliculi

AIM: To investigate the variation of IGSF3 gene in three families with congenital absence of lacrimal puncta and canaliculi, and to lay a foundation for further research on the pathogenic gene of congenital lacrimal duct agenesis. METHODS: The members of the three families were recruited. The ophtha...

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Detalhes bibliográficos
Publicado no:Int J Ophthalmol
Main Authors: Wang, Fei, Tao, Hai, Han, Cui, Bai, Fang, Wang, Peng, Zhou, Xi-Bin, Wang, Li-Hua, Liu, Chuan
Formato: Artigo
Idioma:Inglês
Publicado em: International Journal of Ophthalmology Press 2020
Assuntos:
Basic Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7459218/
https://ncbi.nlm.nih.gov/pubmed/32953570
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18240/ijo.2020.09.02
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