A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.

Human mutation

Volumn 19, Issue 4, 2002, Pages 462-

  Heathcott, Rosemary W ^a   Morison, Ian M ^a   Gubler, Marie Claire ^a   Corbett, Robin ^a   Reeve, Anthony E ^a  

^a UNIVERSITY OF OTAGO   (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

WT1 PROTEIN; ZINC FINGER PROTEIN;

ALTERNATIVE RNA SPLICING; CASE REPORT; CHEMISTRY; DENYS DRASH SYNDROME; FEMALE; GENETICS; HUMAN; MUTATION; PATHOLOGY; PATHOPHYSIOLOGY; PHENOTYPE; REVIEW; STOP CODON; TUMOR SUPPRESSOR GENE;

ALTERNATIVE SPLICING; CODON, NONSENSE; DENYS-DRASH SYNDROME; FEMALE; GENES, WILMS TUMOR; GERM-LINE MUTATION; HUMANS; PHENOTYPE; WT1 PROTEINS; ZINC FINGERS;

EID: 2542500349     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9031     Document Type: Review

References (14)