A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental Isodisomy.
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| Title: | A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental Isodisomy. |
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| Authors: | Lee, Hane1 (AUTHOR), Moon, Dongseok1 (AUTHOR), Khang, Rin1 (AUTHOR), Seo, Go Hun1 (AUTHOR), Yoon, Chang Ki2 (AUTHOR), Park, Un Chul2 (AUTHOR), Park, Kyu Hyung2 (AUTHOR) jiani4@snu.ac.kr, Lee, Eun Kyoung2 (AUTHOR) right184@snu.ac.kr |
| Source: | Molecular Genetics & Genomic Medicine. Jan2025, Vol. 13 Issue 1, p1-6. 6p. |
| Database: | Academic Search Ultimate |
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