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Details on Person Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
| Class:Id | LiteratureReference:1637876 |
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| _displayName | Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome |
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| _timestamp | 2011-10-05 18:32:35 |
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| author | [Person:1008205] Wilkie, AO
[Person:1614761] Slaney, SF
[Person:1614753] Oldridge, M
[Person:1614754] Poole, MD
[Person:1614744] Ashworth, GJ
[Person:1614751] Hockley, AD
[Person:1614749] Hayward, RD
[Person:1614747] David, DJ
[Person:1614756] Pulleyn, LJ
[Person:1614759] Rutland, P |
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| created | [InstanceEdit:1637875] Rothfels, K, 2011-10-05 |
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| journal | Nat Genet |
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| pages | 165-72 |
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| pubMedIdentifier | 7719344 |
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| title | Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome |
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| volume | 9 |
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| year | 1995 |
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| (literatureReference) | [EntityWithAccessionedSequence:1637916] FGFR2c P253R [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2011846] FGFR2b S252W [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2011851] FGFR2b P253R [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2011852] FGFR2c S252W [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2011874] p-8Y-FGFR2b S252W [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2011877] p-8Y-FGFR2b P253R [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2011879] p-8Y-FGFR2c S252W [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2011880] p-8Y-FGFR2c P253R [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2029869] p-8Y-FGFR2b S373C [plasma membrane] [Homo sapiens]
[Reaction:2033472] FGFR2c mutants bind an expanded range of ligands [Homo sapiens] |
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