New case of bilateral pheochromocytomas involving the homozygous TMEM127 mutation

Clin Genet. 2018 Aug;94(2):278-279. doi: 10.1111/cge.13361. Epub 2018 May 11.

Authors

S Laboureau¹, A Guichet², T Duriez³, C Veyrat-Durebex^{2

4}, N Bouzamondo², C Briet¹, D Mirebeau-Prunier^{2

4}

Affiliations

¹ Department of Endocrinology, Centre Hospitalier Universitaire d'Angers, Angers, Pays de la Loire, France.
² Department of Biochemistry and Genetics, CHU Angers, Angers, France.
³ Department of Endocrinology, Cholet Hospital, Cholet, France.
⁴ UMR CNRS 6015- INSERMU1083, University of Angers, Angers, France.

PMID: 29749617
DOI: 10.1111/cge.13361

No abstract available

Publication types

Letter
Comment

MeSH terms

Adrenal Gland Neoplasms*
Homozygote
Humans
Membrane Proteins / genetics
Mutation
Pheochromocytoma*

Substances

Membrane Proteins
TMEM127 protein, human