Literature DB >> 4543597

A family pedigree with corneal dystrophy, tapetoretinal degeneration and albinism.

A Pinckers, A J Otto, J E Van den Heuvel.   

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Year:  1973        PMID： 4543597     DOI： 10.1111/j.1755-3768.1973.tb06024.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN： 0001-639X


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  1 in total

1.  Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosa.

Authors:  Rob W J Collin; Christine Safieh; Karin W Littink; Stavit A Shalev; Hanna J Garzozi; Leah Rizel; Anan H Abbasi; Frans P M Cremers; Anneke I den Hollander; B Jeroen Klevering; Tamar Ben-Yosef
Journal:  Am J Hum Genet       Date:  2010-04-15       Impact factor: 11.025
  1 in total

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