טוען...
Mutation analysis of FBN1 gene in two Chinese families with congenital ectopia lentis in northern China
AIM: To summarize the phenotypes and identify the underlying genetic cause of the fibrillin-1 (FBN1) gene responsible for congenital ectopia lentis (EL) in two Chinese families in northern China. METHODS: A detailed family history and clinical data from all participants were collected by clinical ex...
שמור ב:
| הוצא לאור ב: | Int J Ophthalmol |
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| Main Authors: | , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
International Journal of Ophthalmology Press
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6848879/ https://ncbi.nlm.nih.gov/pubmed/31741853 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18240/ijo.2019.11.02 |
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