Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature.
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Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature.
description
2017 nî lūn-bûn
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2017 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2017年の論文
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2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
name
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@ast
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@en
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@nl
type
label
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@ast
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@en
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@nl
prefLabel
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@ast
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@en
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@nl
P2093
P2860
P50
P356
P1476
Novel PEX11B Mutations Extend ...... Cataract as an Early Feature.
@en
P2093
Alison M Meynert
Charu Deshpande
Christopher Campbell
Deirdre Donnelly
Gisela Wilcox
Helen Mundy
I Chris Lloyd
Jill Clayton-Smith
Jill Urquhart
Rachel L Taylor
P2860
P304
P356
10.1167/IOVS.16-21026
P407
P577
2017-01-01T00:00:00Z