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Details on Person E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency
| Class:Id | LiteratureReference:5601955 |
|---|---|
| _displayName | E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
| _timestamp | 2014-06-16 14:08:13 |
| author | [Person:5601938] Kirby-Keyser, L [Person:5601969] Porter, C C [Person:5601965] Donohoue, P A |
| created | [InstanceEdit:5601985] Jassal, Bijay, 2014-06-16 |
| journal | Hum. Mutat. |
| pages | 181-2 |
| pubMedIdentifier | 9067760 |
| title | E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
| volume | 9 |
| year | 1997 |
| (literatureReference) | [FailedReaction:5601976] Defective CYP21A2 does not 21-hydroxylate PROG [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency (5601955)
