NA16791
DNA from Whole Blood
Description:
ICHTHYOSIS, X-LINKED, WITHOUT STEROID SULFATASE DEFICIENCY
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases |
| Class |
X Chromosome Markers |
| Quantity |
50 µg |
| Quantitation Method |
Please see our FAQ |
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Biopsy Source
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Peripheral vein
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Cell Type
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B-Lymphocyte
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Tissue Type
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Blood
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Transformant
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Epstein-Barr Virus
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Sample Source
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DNA from Whole Blood
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Race
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White
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Ethnicity
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SARDINIAN
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Family Member
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8
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Relation to Proband
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maternal cousin
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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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Note
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This material represents a finite resource (DNA from Whole Blood)
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Remarks
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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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| 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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| Remarks |
Sardinian; clinically status in question; 3 affected brothers (GM16785, GM16788, & GM16789) |
| Robledo R, Melis P, Schillinger E, Casciano I, Balazs I, Rinaldi A, Siniscalco M, Filippi G, X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studies. Am J Med Genet59(2):143-8 1995 |
| PubMed ID: 8588575 |
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