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Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma

✍ Scribed by Cascon, Alberto; Ruiz-Llorente, Sergio; Cebrian, Arancha; Telleria, Dolores; Rivero, Jose Carlos; Diez, Juan Jose; Lopez-Ibarra, Pablo J; Jaunsolo, Miguel Angel; Benitez, Javier; Robledo, Mercedes


Book ID
110025250
Publisher
Nature Publishing Group
Year
2002
Tongue
English
Weight
116 KB
Volume
10
Category
Article
ISSN
1018-4813

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## Abstract Paraganglioma (PGL) is a rare disorder characterized by tumors of the head and neck region. Between 10% and 50% of cases of PGL are familial, and the disease is autosomal dominant and subject to age‐dependent penetrance and imprinting. The paraganglioma gene (__PGL1__) has been mapped t