Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma-Reference-Cited by-同舟云学术

Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma

Published:2003-11-20 Issue:6 Volume:59 Page:707-715
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:

Author:

Opocher G.,Schiavi F.,Vettori A.,Pampinella F.,Vitiello L.,Calderan A.,Vianello B.,Murgia A.,Martella M.,Taccaliti A.,Mantero F.,Mostacciuolo M. L.

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2003.01910.x/fullpdf

Reference28 articles.

1. Germline SDHD mutation in familial phaeochromocytoma;Astuti;The Lancet,2001a

2. Mutations in the mitochondrial complex II subunit SDHB cause susceptibility to familial paraganglioma and pheochromocytoma;Astuti;American Journal of Human Genetics,2001b

3. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma;Baysal;Science,2000

4. Phenotypic dichotomy in mitochondrial complex II genetic disorders;Baysal;Journal of Molecular Medicine,2001

5. Differential Genetic Alterations in von Hippel-Lindau Syndrome-associated and Sporadic Pheochromocytomas;Bender;Journal of Clinical Endocrinology and Metabolism,2000

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