NA09113
DNA from Fibroblast
Description:
GYRATE ATROPHY OF CHOROID AND RETINA; GACR
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases
Disorders of the Urea Cycle |
| Class |
Disorders of Amino Acid Metabolism |
| Quantity |
10 µg |
| Quantitation Method |
Please see our FAQ |
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Cell Type
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Fibroblast
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Transformant
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Untransformed
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Sample Source
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DNA from Fibroblast
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Race
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White
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Relation to Proband
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proband
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Confirmation
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Clinical summary/Case history
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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| Passage Frozen |
15 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis |
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| ornithine aminotransferase |
According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 2.6.1.13; 19% activity. |
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| Remarks |
Pyridoxine responsive; approximately 19% of control fibroblast ornithine aminotransferase activity; not of Finnish extraction; negative family history; mild clinical disease |
| Wirtz MK, Kennaway NG, Weleber RG, Heterogeneity and complementation analysis of fibroblasts from vitamin B6 responsive and non-responsive patients with gyrate atrophy of the choroid and retina. J Inherit Metab Dis8:71-4 1985 |
| PubMed ID: 3939534 |
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| Weleber RG, Wirtz MK, Kennaway NG, Gyrate atrophy of the choroid and retina: clinical and biochemical heterogeneity and response to vitamin B6. Birth Defects Orig Artic Ser18:219-30 1982 |
| PubMed ID: 7171757 |
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| Weleber RG, Kennaway NG, Clinical trial of vitamin B6 for gyrate atrophy of the choroid and retina. Ophthalmology88:316-24 1981 |
| PubMed ID: 6789268 |
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