(PDF) Mutation Analysis of the SDHB and SDHD Genes in

Mutation Analysis of the SDHB and SDHD Genes in Pheochromocytomas and Paragangliomas: Identification of a Novel Nonsense Mutation (Q168X) in the SDHB Gene

Endocrine Journal - Japan

doi 10.1507/endocrj.k10e-023

Full Text

Open PDF

Abstract

Available in full text

Date

January 1, 2010

Authors

Publisher

Japan Endocrine Society

Related search

A Novel SDHB Mutation Associated With Hereditary Head and Neck Paraganglioma

Laryngoscope

Otorhinolaryngology

2011

English

Identification of a Nonsense Mutation in the PAX9 Gene in Molar Oligodontia

European Journal of Human Genetics

Genetics

2001

English

Uncommon Spreading of Primary Malignant Paraganglioma in a Patient With SDHB Mutation

Case Reports in Internal Medicine

2017

English

Tumour Risks and Genotype–phenotype–proteotype Analysis of Patients With Germline Mutations in the Succinate Dehydrogenase Subunit Genes SDHB, SDHC, and SDHD

The Lancet

Medicine

2016

English

R46Q Mutation in the Succinate Dehydrogenase B Gene (SDHB) in a Japanese Family With Both Abdominal and Thoracic Paraganglioma Following Metastasis

English

Paragangliomas Múltiples Asociados a Mutación Del Gen SDHB: Caso Clínico

Revista Medica de Chile

Medicine

2011

English

Plasma Methoxytyramine: A Novel Biomarker of Metastatic Pheochromocytoma and Paraganglioma in Relation to Established Risk Factors of Tumour Size, Location and SDHB Mutation Status

European Journal of Cancer

Cancer Research

Oncology

2012

English

A Novel Nonsense Mutation of the PEPD Gene in a Japanese Patient With Prolidase Deficiency

Journal of Human Genetics

Genetics

2000

English

Cardiac Paraganglioma Arising From the Right Atrioventricular Groove in a Paraganglioma-Pheochromocytoma Family Syndrome With Evidence of SDHB Gene Mutation: An Unusual Presentation

Annals of Thoracic Surgery

Respiratory Medicine

Pulmonary

Cardiovascular Medicine

Surgery

Cardiology

2016

English

Amanote Research

Mutation Analysis of the SDHB and SDHD Genes in Pheochromocytomas and Paragangliomas: Identification of a Novel Nonsense Mutation (Q168X) in the SDHB Gene

Endocrine Journal - Japan

doi 10.1507/endocrj.k10e-023

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

A Novel SDHB Mutation Associated With Hereditary Head and Neck Paraganglioma

Identification of a Nonsense Mutation in the PAX9 Gene in Molar Oligodontia

Uncommon Spreading of Primary Malignant Paraganglioma in a Patient With SDHB Mutation

Tumour Risks and Genotype–phenotype–proteotype Analysis of Patients With Germline Mutations in the Succinate Dehydrogenase Subunit Genes SDHB, SDHC, and SDHD

R46Q Mutation in the Succinate Dehydrogenase B Gene (SDHB) in a Japanese Family With Both Abdominal and Thoracic Paraganglioma Following Metastasis

Paragangliomas Múltiples Asociados a Mutación Del Gen SDHB: Caso Clínico

Plasma Methoxytyramine: A Novel Biomarker of Metastatic Pheochromocytoma and Paraganglioma in Relation to Established Risk Factors of Tumour Size, Location and SDHB Mutation Status

A Novel Nonsense Mutation of the PEPD Gene in a Japanese Patient With Prolidase Deficiency

Cardiac Paraganglioma Arising From the Right Atrioventricular Groove in a Paraganglioma-Pheochromocytoma Family Syndrome With Evidence of SDHB Gene Mutation: An Unusual Presentation