Entries of Weinitz, Silke on the publication server
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2017
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.
(2017)
Mevalonate kinase deficiency associated with ataxia and retinitis pigmentosa in two brothers with MVK gene mutations.
Ophthalmic Genetics.
Fulltext not available.