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Volumn 23, Issue 5, 2014, Pages 366-368
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Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing
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Author keywords
[No Author keywords available]
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Indexed keywords
EPHRIN RECEPTOR A7;
STAT4 PROTEIN;
CELL CYCLE PROTEIN;
CELL RECEPTOR;
NUCLEAR PROTEIN;
REPRESSOR PROTEIN;
TBL1XR1 PROTEIN, HUMAN;
APOPTOSIS;
BLOOD SAMPLING;
CANCER DIAGNOSIS;
CELL MATURATION;
CHROMOSOME 17Q;
CHROMOSOME 8;
CONTROLLED STUDY;
COPY NUMBER VARIATION;
GENE;
GENE EXPRESSION;
GENE SEQUENCE;
HETEROZYGOSITY LOSS;
HUMAN;
LETTER;
MISSENSE MUTATION;
MYCOSIS FUNGOIDES;
SEZARY SYNDROME;
SLFN12 GENE;
SOMATIC MUTATION;
T LYMPHOCYTE;
TBL1XR1 GENE;
COHORT ANALYSIS;
CYTOLOGY;
DNA SEQUENCE;
EXOME;
GENE DELETION;
GENE EXPRESSION PROFILING;
GENETICS;
HETEROZYGOTE;
MALE;
MIDDLE AGED;
MUTATION;
APOPTOSIS;
CELL CYCLE PROTEINS;
COHORT STUDIES;
DNA COPY NUMBER VARIATIONS;
EXOME;
GENE DELETION;
GENE EXPRESSION PROFILING;
HETEROZYGOTE;
HUMANS;
MALE;
MIDDLE AGED;
MUTATION;
MUTATION, MISSENSE;
NUCLEAR PROTEINS;
RECEPTOR, EPHA7;
RECEPTORS, CYTOPLASMIC AND NUCLEAR;
REPRESSOR PROTEINS;
SEQUENCE ANALYSIS, DNA;
SEZARY SYNDROME;
T-LYMPHOCYTES;
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EID: 84899550326
PISSN: 09066705
EISSN: 16000625
Source Type: Journal
DOI: 10.1111/exd.12405 Document Type: Letter |
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Times cited : (12)
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References (20)
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