Hereditas

ISSN	1601-5223
ISSN-L	0018-0661
IUID	5451d972f20942b18a61116d450ef6e6
Modified	2020-11-27T13:14:06.041Z
Created	2018-10-29T14:32:23.521Z

Year 2017

PubMed DOI Crossref

Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes.

Olsson KS, Wålinder O, Jansson U, ..., Raha-Chowdhury R, Williams R

Hereditas 154 (1) 16 [2017-12-19; online 2017-12-19]

Clinical Genomics Uppsala [Collaborative]

SciLifeLab Data Centre

Publications 9.5.1