Different phenotypes of lattice corneal dystrophy type I in patients with 417C>T (R124C) and 1762A>G (H572R) mutations in TGFBI (BIGH3).
about
Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy.pH Induced Conformational Transitions in the Transforming Growth Factor β-Induced Protein (TGFβIp) Associated Corneal Dystrophy Mutants.Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy.
P2860
Different phenotypes of lattice corneal dystrophy type I in patients with 417C>T (R124C) and 1762A>G (H572R) mutations in TGFBI (BIGH3).
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Different phenotypes of lattic ...... R) mutations in TGFBI (BIGH3).
@ast
Different phenotypes of lattic ...... R) mutations in TGFBI (BIGH3).
@en
Different phenotypes of lattice corneal dystrophy type I in patients with 417C>T
@nl
type
label
Different phenotypes of lattic ...... R) mutations in TGFBI (BIGH3).
@ast
Different phenotypes of lattic ...... R) mutations in TGFBI (BIGH3).
@en
Different phenotypes of lattice corneal dystrophy type I in patients with 417C>T
@nl
prefLabel
Different phenotypes of lattic ...... R) mutations in TGFBI (BIGH3).
@ast
Different phenotypes of lattic ...... R) mutations in TGFBI (BIGH3).
@en
Different phenotypes of lattice corneal dystrophy type I in patients with 417C>T
@nl
P2093
P2860
P1433
P1476
Different phenotypes of lattic ...... R) mutations in TGFBI (BIGH3).
@en
P2093
Luisa Herrera
Mauricio Moraga
Pablo Romero
P2860
P304
P577
2010-08-13T00:00:00Z