دورية أكاديمية
Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene
| العنوان: | Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene |
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| المؤلفون: | Chograni, M., Alahdal, H. M.Aff2, IDs40246023004926_cor2, Rejili, M. |
| المصدر: | Human Genomics. 17(1) |
| قاعدة البيانات: | Springer Nature Journals |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 14797364 |
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| DOI: | 10.1186/s40246-023-00492-6 |