Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies.
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Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies.
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2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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name
Founder Effect of a c.828+3A>T ...... Dominant Retinal Dystrophies.
@ast
Founder Effect of a c.828+3A>T ...... Dominant Retinal Dystrophies.
@en
type
label
Founder Effect of a c.828+3A>T ...... Dominant Retinal Dystrophies.
@ast
Founder Effect of a c.828+3A>T ...... Dominant Retinal Dystrophies.
@en
prefLabel
Founder Effect of a c.828+3A>T ...... Dominant Retinal Dystrophies.
@ast
Founder Effect of a c.828+3A>T ...... Dominant Retinal Dystrophies.
@en
P2093
P2860
P1433
P1476
Founder Effect of a c.828+3A&g ...... Dominant Retinal Dystrophies.
@en
P2093
David G Birch
Dianna K Hughbanks-Wheaton
Lori S Sullivan
Richard S Ruiz
Sara J Bowne
Suma P Shankar
P2860
P304
P356
10.1001/JAMAOPHTHALMOL.2014.6115
P407
P577
2015-05-01T00:00:00Z