Novel mutations and the emergence of a common mutation in theSDHD gene causing familial paraganglioma
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference19 articles.
1. Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma
2. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia
3. Familial carotid body tumors: Case report and epidemiologic review
4. A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter
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5. The spectrum of SDHD mutations in Russian patients with head and neck paraganglioma;International Journal of Neuroscience;2018-10-30
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