Human Genome Epidemiology Literature Finder
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Query Trace: Leber Congenital Amaurosis and TULP1[original query] |
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The genetic aetiology of retinal degeneration in children in Finland - new founder mutations identified. Acta ophthalmologica 2019 May . Avela Kristiina, Salonen-Kajander Riitta, Laitinen Arja, Ramsden Simon, Barton Stephanie, Rudanko Sirkka-Lii |
- Page last reviewed:Feb 1, 2024
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