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Extending the phenotype of midface toddler excoriation syndrome (MiTES): Five new cases in three families with PR domain containing protein 12 (PRDM12) mutations. (2019)

First Author: Inamadar AC

Attributed to: Use of patient mis sense mutations in SCN9A to increase our understanding of the structure and function of sodium channels funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.jaad.2019.05.036

PubMed Identifier: 31128170

Publication URI: http://europepmc.org/abstract/MED/31128170

Type: Journal Article/Review

Volume: 81

Parent Publication: Journal of the American Academy of Dermatology

Issue: 6

ISSN: 0190-9622