NRAS mutations in Noonan syndrome

Molecular Syndromology

Volumn 3, Issue 1, 2012, Pages 34-38

  Denayer, E ^a   Peeters, H ^a   Sevenants, L ^a   Derbent, M ^b   Fryns, J P ^a   Legius, E ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b BASKENT UNIVERSITY   (Turkey)

Author keywords

Noonan syndrome; NRAS; RAS MAPK pathway

Indexed keywords

COMPLEMENTARY DNA; MITOGEN ACTIVATED PROTEIN KINASE; RAS PROTEIN;

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; CHILD; CODON; CONGENITAL HEART MALFORMATION; CRYPTORCHISM; DELAYED PUBERTY; FACE MALFORMATION; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; HUMAN; MALE; NOONAN SYNDROME; NRAS GENE; NUCLEOTIDE SEQUENCE; PEDIGREE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; SHORT STATURE;

EID: 84862494077     PISSN: 16618769     EISSN: 16618777     Source Type: Journal    
DOI: 10.1159/000338467     Document Type: Article

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