Structural Analysis of G1691S Variant in the Human Filamin B Gene Responsible for Larsen Syndrome: A Comparative Computational Approach.
about
Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach.Genotype-phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants.Comparative computational assessment of the pathogenicity of mutations in the Aspartoacylase enzyme.
P2860
Structural Analysis of G1691S Variant in the Human Filamin B Gene Responsible for Larsen Syndrome: A Comparative Computational Approach.
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-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
2017年學術文章
@zh-hant
name
Structural Analysis of G1691S ...... rative Computational Approach.
@en
Structural Analysis of G1691S ...... rative Computational Approach.
@nl
type
label
Structural Analysis of G1691S ...... rative Computational Approach.
@en
Structural Analysis of G1691S ...... rative Computational Approach.
@nl
prefLabel
Structural Analysis of G1691S ...... rative Computational Approach.
@en
Structural Analysis of G1691S ...... rative Computational Approach.
@nl
P2093
P2860
P50
P356
P1476
Structural Analysis of G1691S ...... arative Computational Approach
@en
P2093
Himani Tanwar
Kumar Thirumal D
P2860
P304
P356
10.1002/JCB.25920
P577
2017-03-27T00:00:00Z