Lack of GNAQ germline mutations in uveal melanoma patients with high risk for hereditary cancer predisposition

Familial Cancer

Volumn 10, Issue 2, 2011, Pages 319-321

  Abdel Rahman, Mohamed H ^a,b   Pilarski, Robert ^b   Massengill, James B ^a   Christopher, Benjamin B ^a   Davidorf, Frederick H ^a  

^a OHIO STATE UNIVERSITY   (United States)

^b OHIO STATE UNIVERSITY   (United States)

Author keywords

Eye neoplasm; Familial cancer; GNAQ; Uveal melanoma

Indexed keywords

ARTICLE; CANCER PATIENT; CANCER SUSCEPTIBILITY; CLINICAL ARTICLE; EXON; FAMILIAL CANCER; FAMILY HISTORY; GENE FREQUENCY; GENE SEQUENCE; GENETIC SCREENING; GENETIC VARIABILITY; GERM LINE; GNAQ GENE; HIGH RISK PATIENT; HUMAN; HUMAN TISSUE; INTRON; MUTATION RATE; ONCOGENE; ONSET AGE; PRIORITY JOURNAL; SOMATIC MUTATION; UVEA MELANOMA;

GENETIC PREDISPOSITION TO DISEASE; GERM-LINE MUTATION; GTP-BINDING PROTEIN ALPHA SUBUNITS; HUMANS; INTRONS; MELANOMA; UVEAL NEOPLASMS;

EID: 79958172913     PISSN: 13899600     EISSN: 15737292     Source Type: Journal    
DOI: 10.1007/s10689-010-9401-2     Document Type: Article

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