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Oxford University Press

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Sprouty Proteins, A New Family of Receptor Tyrosine Kinase Inhibitors

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Bentham Science Publishers

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Coats’ disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis

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Human Molecular Genetics, Vol. 8, Iss. 11, 1999-10 ,pp. : 2031-2035

Oxford University Press

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A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population

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Springer Publishing Company

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Recessively Inherited L-DOPA-Responsive Parkinsonism In Infancy Caused by A Point Mutation (L205p) in the Tyrosine Hydroxylase Gene

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Oxford University Press

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