Extending the phenotype of midface toddler excoriation syndrome (MiTES): Five new cases in three families with PR domain containing protein 12 (PRDM12) mutations. (2019)
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/10.17863/cam.40787
Publication URI: https://www.repository.cam.ac.uk/handle/1810/293675
Type: Journal Article/Review