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.
about
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.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh-hant
name
Common founder effects of here ...... ns in the WHRN and TMC1 genes.
@en
Common founder effects of here ...... ns in the WHRN and TMC1 genes.
@nl
type
label
Common founder effects of here ...... ns in the WHRN and TMC1 genes.
@en
Common founder effects of here ...... ns in the WHRN and TMC1 genes.
@nl
prefLabel
Common founder effects of here ...... ns in the WHRN and TMC1 genes.
@en
Common founder effects of here ...... ns in the WHRN and TMC1 genes.
@nl
P2093
P2860
P1433
P1476
Common founder effects of here ...... ns in the WHRN and TMC1 genes.
@en
P2093
Eva-Lena Stattin
K Sigvard Olsson
Maria Wilbe
Marie-Louise Bondeson
Olof Wålinder
Roger Williams
Ruma Raha-Chowdhury
Ulf Jansson
P2860
P2888
P356
10.1186/S41065-017-0052-2
P577
2017-12-19T00:00:00Z
P6179
1099725231