A Novel Double RET E768D/L790F Mutation Associated with a MEN2B-Like Phenotype-Reference-Cited by-同舟云学术

A Novel Double RET E768D/L790F Mutation Associated with a MEN2B-Like Phenotype

Published:2021-02-01 Issue:2 Volume:31 Page:327-329
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Mathew Annie¹,Latteyer Soeren¹,Frank-Raue Karin²,Moeller Lars C.¹,Zwanziger Denise¹,Mengel Manuel³,Führer Dagmar¹,Tiedje Vera¹

Affiliation:

1. Department of Endocrinology, Diabetes and Metabolism and Division of Laboratory Research, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

2. Endocrine Practice Heidelberg, Molecular Genetic Laboratory, Heidelberg, Germany.

3. Endocrine Practice, Wuppertal, Germany.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2019.0472

Reference4 articles.

1. Long-Term Survivorship in Multiple Endocrine Neoplasia Type 2B Diagnosed Before and in the New Millennium

2. Advances in the management of MEN2: from improved surgical and medical treatment to novel kinase inhibitors

3. A 6-Base Pair in Frame Germline Deletion in Exon 7 Of RET Leads to Increased RET Phosphorylation, ERK Activation, and MEN2A

4. Revised American Thyroid Association Guidelines for the Management of Medullary Thyroid Carcinoma

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