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Germline Mutation of von Hippel–Lindau (VHL) Gene 695 G>A (R161Q) in a Patient with a Peculiar Phenotype with Type 2C VHL Syndrome
LIBERO SANTARPIA, DANIELA LAPA, SALVATORE BENVENGAVolume:
1073
Year:
2006
Language:
english
Pages:
5
DOI:
10.1196/annals.1353.021
File:
PDF, 126 KB
english, 2006