Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing.
about
The mutational landscape of ocular marginal zone lymphoma identifies frequent alterations in TNFAIP3 followed by mutations in TBL1XR1 and CREBBP.TBL1XR1 in physiological and pathological statesA specific mutation in TBL1XR1 causes Pierpont syndrome.Genomic analyses reveal recurrent mutations in epigenetic modifiers and the JAK-STAT pathway in Sézary syndromeDifferent genetic alteration of A20 in a Sézary syndrome case with Vα2-Jα22 T cell clone.
P2860
Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing.
description
2014 nî lūn-bûn
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2014年の論文
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name
Novel TBL1XR1, EPHA7 and SLFN1 ...... red by whole exome sequencing.
@en
Novel TBL1XR1, EPHA7 and SLFN1 ...... red by whole exome sequencing.
@nl
type
label
Novel TBL1XR1, EPHA7 and SLFN1 ...... red by whole exome sequencing.
@en
Novel TBL1XR1, EPHA7 and SLFN1 ...... red by whole exome sequencing.
@nl
prefLabel
Novel TBL1XR1, EPHA7 and SLFN1 ...... red by whole exome sequencing.
@en
Novel TBL1XR1, EPHA7 and SLFN1 ...... red by whole exome sequencing.
@nl
P2093
P2860
P50
P356
P1476
Novel TBL1XR1, EPHA7 and SLFN1 ...... red by whole exome sequencing.
@en
P2093
Annamari Ranki
Henrik Edgren
Liisa Väkevä
P2860
P304
P356
10.1111/EXD.12405
P577
2014-05-01T00:00:00Z