Literature DB >> 8542823

[Hyperornithinemia and gyrate atrophy: ornithine aminotransferase gene error causing a Finnish disease].

I Sipilä1, D Valle, G A Mitchell, L C Brody.   

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Year:  1994        PMID： 8542823

Source DB:  PubMed          Journal:  Duodecim        ISSN： 0012-7183


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  2 in total

1.  Retinal detachment causing unilateral blindness in a 12-year-old girl with gyrate atrophy.

Authors:  C P Barnett; W-C Lam; A Schulze
Journal:  J Inherit Metab Dis       Date:  2009-10       Impact factor: 4.982

2.  Gyrate atrophy of the choroid and retina with hyperornithinemia, cystinuria and lysinuria responsive to vitamin B6.

Authors:  Fatos Tanzer; Mehtap Firat; Meral Alagoz; Haydar Erdogan
Journal:  BMJ Case Rep       Date:  2011-03-15
  2 in total

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