Genetic basis of endocrine disease: multiple endocrine neoplasia type 2.

Lois M. Mulligan; B. A. J. Ponder

doi:10.1210/jcem.80.7.7608246

July 1, 1995The Journal of Clinical Endocrinology & Metabolism

Genetic basis of endocrine disease: multiple endocrine neoplasia type 2.

View at Publisher

Ask AI

Bookmark

Share

Key Points

The research aims to explore the genetic factors contributing to multiple endocrine neoplasia type 2.
Examined genetic mutations in patients with multiple endocrine neoplasia type 2
Identified relevant tumor syndromes
Analyzed patient data from clinical sources
Identified specific mutations that significantly increase the risk of developing multiple endocrine neoplasia type 2
Findings suggest a strong genetic link with a particular focus on RET mutations

Ask about this paper

Answers are grounded in this paper and cite their sources.

Implication

Reveals genetic mutations associated with endocrine disease, indicating implications for diagnosis and treatment.

Abstract

L M Mulligan, B A Ponder; Genetic basis of endocrine disease: multiple endocrine neoplasia type 2, The Journal of Clinical Endocrinology & Metabolism, Volume 80

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Mulligan et al. (1995) studied this question.

synapsesocial.com/papers/6a70f3952163a0a01bc52701 https://doi.org/10.1210/jcem.80.7.7608246

View at Publisher

Ask AI

Bookmark

Share

Genetic basis of endocrine disease: multiple endocrine neoplasia type 2.

Key Points

Ask about this paper

Implication

Abstract

Discussion

Cite This Study

Genetic basis of endocrine disease: multiple endocrine neoplasia type 2.

Key Points

Ask about this paper

Implication

Abstract

Discussion

Cite This Study

Keep reading

Keep reading