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Details on Person Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3
| Class:Id | LiteratureReference:216607 |
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| _displayName | Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3 |
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| _timestamp | 2016-09-24 16:57:26 |
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| author | [Person:163404] Lefevre, C
[Person:163394] Bouadjar, B
[Person:216619] Ferrand, Véronique
[Person:216573] Tadini, Gianluca
[Person:2730971] Megarbane, André
[Person:163479] Lathrop, M
[Person:163540] Prud'homme, JF
[Person:163494] Fischer, J |
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| created | [InstanceEdit:216615] Jassal, B, 2008-03-18 13:03:19 |
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| journal | Hum Mol Genet |
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| modified | [InstanceEdit:216640] Jassal, B, 2008-03-18 13:06:36
[InstanceEdit:8940281] D'Eustachio, Peter, 2016-09-24 |
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| pages | 767-76 |
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| pubMedIdentifier | 16436457 |
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| title | Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3 |
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| volume | 15 |
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| year | 2006 |
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| (literatureReference) | [Reaction:211902] Orphan CYP4F22 [Homo sapiens]
[Pathway:5579005] Defective CYP4F22 causes ARCI5 [Homo sapiens]
[FailedReaction:5602272] Defective CYP4F22 does not 20-hydroxylate TrXA3 [Homo sapiens]
[Reaction:5602295] CYP4F22 20-hydroxylates TrXA3 [Homo sapiens] |
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