Hereditary paraganglioma due to the SDHD M1I mutation in a second chinese family: A founder effect?

Laryngoscope

Volumn 113, Issue 6, 2003, Pages 1055-1058

  Lee, Soo Chin ^a   Chionh, Siok Bee ^a   Chong, Siew Meng ^a   Taschner, Peter E M ^a,b  

^a NATIONAL UNIVERSITY HOSPITAL   (Singapore)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Chinese; Hereditary paraganglioma; Hereditary paraganglioma syndrome PGL1; Pheochromocytoma; SDHD

Indexed keywords

ADULT; ARTICLE; AUSTRALIA; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHINESE; CHROMOSOME 11Q; FAMILY; FEMALE; GENE; GENE LOCUS; GENE MUTATION; GENETIC CODE; HEAD TUMOR; HUMAN; MALE; MITOCHONDRIAL RESPIRATION; NECK TUMOR; PARAGANGLIOMA; PHEOCHROMOCYTOMA; PRIORITY JOURNAL; RESPIRATORY CHAIN; SDHB GENE; SDHC GENE; SDHD M11 GENE; START CODON;

ADRENAL GLAND NEOPLASMS; ADULT; AGED; AMINO ACID SUBSTITUTION; ASIAN CONTINENTAL ANCESTRY GROUP; CAROTID BODY; CHINA; CHROMOSOME ABERRATIONS; CODON; DNA MUTATIONAL ANALYSIS; ELECTRON TRANSPORT COMPLEX II; FEMALE; FOUNDER EFFECT; GENES, DOMINANT; GLOMUS JUGULARE TUMOR; HEAD AND NECK NEOPLASMS; HETEROZYGOTE DETECTION; HUMANS; IRON-SULFUR PROTEINS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MULTIENZYME COMPLEXES; NEOPLASMS, MULTIPLE PRIMARY; OXIDOREDUCTASES; PARAGANGLIOMA; PEDIGREE; PHEOCHROMOCYTOMA; PROTEIN SUBUNITS; SINGAPORE; SUCCINATE DEHYDROGENASE;

EID: 0037646095     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005537-200306000-00026     Document Type: Article

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