Characterization of the largest kindred with MEN2A due to a Cys609Ser RET mutation

Familial Cancer

Volumn 8, Issue 4, 2009, Pages 379-382

  Mian, Caterina ^a   Barollo, Susi ^b   Zambonin, Laura ^a   Pennelli, Gianmaria ^b   Bernante, Paolo ^a   Pelizzo, Maria Rosa ^a   Nacamulli, Davide ^a   Mantero, Franco ^a   Girelli, Maria Elisa ^a   Opocher, Giuseppe ^a,b  

^a UNIVERSITY OF PADOVA   (Italy)

^b VENETO INSTITUTE OF ONCOLOGY IOV IRCCS   (Italy)

Author keywords

Medullary thyroid carcinoma; MEN2A; Pheochromocytoma; RET

Indexed keywords

CALCITONIN; CYSTEINE; PENTAGASTRIN; PROTEIN RET; SERINE;

ADULT; ARTICLE; CANCER SUSCEPTIBILITY; CASE REPORT; DISTANT METASTASIS; GENE MUTATION; HUMAN; LYMPH NODE METASTASIS; MALE; PENETRANCE; PHEOCHROMOCYTOMA; POINT MUTATION; PRIMARY HYPERPARATHYROIDISM; PRIORITY JOURNAL; SIPPLE SYNDROME; THYROID MEDULLARY CARCINOMA;

ADOLESCENT; ADRENAL GLAND NEOPLASMS; ADULT; FEMALE; HUMANS; HYPERPARATHYROIDISM; MALE; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A; PEDIGREE; PENETRANCE; PHEOCHROMOCYTOMA; POINT MUTATION; PROTO-ONCOGENE PROTEINS C-RET; THYROID NEOPLASMS; YOUNG ADULT;

EID: 70449526559     PISSN: 13899600     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10689-009-9250-z     Document Type: Article

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