A new compound heterozygous mutation (W17X, 436 + 5G --> T) in the cytochrome P450c17 gene causes 17 alpha-hydroxylase/17,20-lyase deficiency
| author | |
| created | [InstanceEdit:5601814] Jassal, Bijay, 2014-06-13 |
| dbId | 5601779 |
| displayName | A new compound heterozygous mutation (W17X, 436 + 5G --> T) in the cytochrome P450c17 gene causes 17 alpha-hydroxylase/17,20-lyase deficiency |
| journal | J. Clin. Endocrinol. Metab. |
| pages | 199-202 |
| pubMedIdentifier | 9435441 |
| schemaClass | LiteratureReference |
| title | A new compound heterozygous mutation (W17X, 436 + 5G --> T) in the cytochrome P450c17 gene causes 17 alpha-hydroxylase/17,20-lyase deficiency |
| url | http://www.ncbi.nlm.nih.gov/pubmed/9435441 |
| volume | 83 |
| year | 1998 |
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