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Volumn 15, Issue 4, 2000, Pages 389-
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Novel WT1 exon 9 mutation (D396Y) in a patient with early onset Denys Drash syndrome.
a
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Author keywords
[No Author keywords available]
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Indexed keywords
ASPARTIC ACID;
DNA BINDING PROTEIN;
TRANSCRIPTION FACTOR;
TYROSINE;
WT1 PROTEIN;
AMINO ACID SUBSTITUTION;
ARTICLE;
CASE REPORT;
EXON;
FATALITY;
GENETICS;
HUMAN;
MALE;
MISSENSE MUTATION;
NEWBORN;
PRESCHOOL CHILD;
SYNDROME;
TUMOR SUPPRESSOR GENE;
UROGENITAL TRACT MALFORMATION;
AMINO ACID SUBSTITUTION;
ASPARTIC ACID;
CHILD, PRESCHOOL;
DNA-BINDING PROTEINS;
EXONS;
FATAL OUTCOME;
GENES, WILMS TUMOR;
HUMANS;
INFANT, NEWBORN;
MALE;
MUTATION, MISSENSE;
SYNDROME;
TRANSCRIPTION FACTORS;
TYROSINE;
UROGENITAL ABNORMALITIES;
WT1 PROTEINS;
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EID: 0034164478
PISSN: None
EISSN: 10981004
Source Type: Journal
DOI: 10.1002/(SICI)1098-1004(200004)15:4<389::AID-HUMU29>3.0.CO;2-E Document Type: Article |
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Times cited : (3)
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References (0)
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