Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.
about
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
Exome sequencing identifies a ...... model for skeletal dysplasia.
@en
Exome sequencing identifies a ...... model for skeletal dysplasia.
@nl
type
label
Exome sequencing identifies a ...... model for skeletal dysplasia.
@en
Exome sequencing identifies a ...... model for skeletal dysplasia.
@nl
prefLabel
Exome sequencing identifies a ...... model for skeletal dysplasia.
@en
Exome sequencing identifies a ...... model for skeletal dysplasia.
@nl
P2093
P2860
P50
P1433
P1476
Exome sequencing identifies a ...... e model for skeletal dysplasia
@en
P2093
Bettina Lorenz-Depiereux
Birgit Mentrup
Birgit Rathkolb
Elisabeth Graf
Franz Jakob
Helmut Fuchs
Marion Horsch
Sibylle Sabrautzki
Sieglinde Bayer
Susanne Diener
P2860
P2888
P304
P356
10.1007/S00335-016-9619-X
P577
2016-01-23T00:00:00Z