Suggestive association with ocular phoria at chromosome 6p22.
about
Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolismMGST2 and WNT2 are candidate genes for comitant strabismus susceptibility in Japanese patients.Individual differences in visual science: What can be learned and what is good experimental practice?Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect
P2860
Suggestive association with ocular phoria at chromosome 6p22.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh-hant
name
Suggestive association with ocular phoria at chromosome 6p22.
@en
Suggestive association with ocular phoria at chromosome 6p22.
@nl
type
label
Suggestive association with ocular phoria at chromosome 6p22.
@en
Suggestive association with ocular phoria at chromosome 6p22.
@nl
prefLabel
Suggestive association with ocular phoria at chromosome 6p22.
@en
Suggestive association with ocular phoria at chromosome 6p22.
@nl
P50
P356
P1476
Suggestive association with ocular phoria at chromosome 6p22.
@en
P2093
Adam J Lawrance-Owen
Gary Bargary
P304
P356
10.1167/IOVS.13-12879
P407
P577
2014-01-20T00:00:00Z