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Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.

• Authors : Schatz P; Department of Ophthalmology, Lund University Hospital, Lund, Sweden. ; Ponjavic V

Subjects: Point Mutation*; IMP Dehydrogenase/IMP Dehydrogenase/IMP Dehydrogenase/*genetics ; Retinitis Pigmentosa/Retinitis Pigmentosa/Retinitis Pigmentosa/*genetics

• Source: Ophthalmic genetics [Ophthalmic Genet] 2005 Sep; Vol. 26 (3), pp. 119-24.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print Cited Medium: Print ISSN: 1381-6810

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