Literature DB >> 1427882

Three novel mutations of the ornithine aminotransferase (OAT) gene in gyrate atrophy.

J K Park1, B J Herron, J J O'Donnell, V E Shih, V Ramesh.   

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Year:  1992        PMID： 1427882     DOI： 10.1016/s0888-7543(05)80271-x

Source DB:  PubMed          Journal:  Genomics        ISSN： 0888-7543            Impact factor:   5.736


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  2 in total

Review 1.  Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.

Authors:  P J Rosenfeld; V A McKusick; J S Amberger; T P Dryja
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

2.  Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226V.

Authors:  J Michaud; G N Thompson; L C Brody; G Steel; C Obie; G Fontaine; K Schappert; C G Keith; D Valle; G A Mitchell
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025
  2 in total

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