Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism. (2018)
Attributed to:
Enabling technologies
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.17863/cam.33608
Publication URI: https://www.repository.cam.ac.uk/handle/1810/286298
Type: Journal Article/Review