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Publications by Weinitz, Silke

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Kellner, Ulrich, Stöhr, Heidi, Weinitz, Silke, Farmand, Ghazaleh and Weber, Bernhard H. F. (2017) Mevalonate kinase deficiency associated with ataxia and retinitis pigmentosa in two brothers with MVK gene mutations. Ophthalmic Genetics. Fulltext not available.

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