Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers.
about
Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Autosomal Dominant Retinal Dys ...... lotypes in trans as Modifiers.
@ast
Autosomal Dominant Retinal Dys ...... lotypes in trans as Modifiers.
@en
type
label
Autosomal Dominant Retinal Dys ...... lotypes in trans as Modifiers.
@ast
Autosomal Dominant Retinal Dys ...... lotypes in trans as Modifiers.
@en
prefLabel
Autosomal Dominant Retinal Dys ...... lotypes in trans as Modifiers.
@ast
Autosomal Dominant Retinal Dys ...... lotypes in trans as Modifiers.
@en
P2093
P2860
P356
P1476
Autosomal Dominant Retinal Dys ...... lotypes in trans as Modifiers.
@en
P2093
David G Birch
Dianna K Hughbanks-Wheaton
Karen N Conneely
Lori S Sullivan
Sara J Bowne
Suma P Shankar
P2860
P304
P356
10.1167/IOVS.15-16965
P407
P577
2016-02-01T00:00:00Z