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Article

Comprehensive Mutation Scanning of NF1 in Apparently Sporadic Cases of Pheochromocytoma

21 Jun 2006

Abstract excerpt

BACKGROUND: Pheochromocytoma is a rare manifestation in patients with neurofibromatosis type 1 (NF 1). The 57-exon susceptibility gene NF1 has so far not been systematically scanned for unexpected germline mutations in individuals with sporadic pheochromocytoma. METHODS: Twenty-seven patients with bilateral adrenal and/or extraadrenal abdominal pheochromocytoma not carrying germline mutations of the genes VHL,...

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PMID: 16787982
DOI: 10.1210/jc.2006-0780

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Comprehensive Mutation Scanning of NF1 in Apparently Sporadic Cases of PheochromocytomaPMID 16787982Read ↗

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