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Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship?
Author(s) -
Bertola DR,
Pereira AC,
Brasil AS,
Suzuki L,
Leite C,
Falzoni R,
Tannuri U,
Poplawski AB,
Janowski KM,
Kim CA,
Messiaen LM
Publication year - 2012
Publication title -
clinical genetics
Language(s) - Norwegian
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2011.01764.x
Subject(s) - kras , medicine , medical genetics , pediatrics , genetics , biology , cancer , gene , colorectal cancer
Univ São Paulo, Fac Med, Unidade Genet, Inst Crianca, São Paulo, BrazilUniv São Paulo, Fac Med, InCor, São Paulo, BrazilUniv São Paulo, Fac Med, Dept Radiol, São Paulo, BrazilUniv São Paulo, Fac Med, Dept Pathol, São Paulo, BrazilUniv São Paulo, Fac Med, Dept Pediat, São Paulo, BrazilUniv Alabama Birmingham, Med Genet Lab, Dept Genet, Birmingham, AL 35294 USAWeb of Scienc