Corneal endothelial findings in a Czech patient with compound heterozygous mutations in KERA.
about
Mutation in KERA identified by linkage analysis and targeted resequencing in a pedigree with premature atherosclerosis.Case report: a novel KERA mutation associated with cornea plana and its predicted effect on protein function.Analysis of KERA in four families with cornea plana identifies two novel mutations.
P2860
Corneal endothelial findings in a Czech patient with compound heterozygous mutations in KERA.
description
2013 nî lūn-bûn
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name
Corneal endothelial findings i ...... eterozygous mutations in KERA.
@en
Corneal endothelial findings i ...... eterozygous mutations in KERA.
@nl
type
label
Corneal endothelial findings i ...... eterozygous mutations in KERA.
@en
Corneal endothelial findings i ...... eterozygous mutations in KERA.
@nl
prefLabel
Corneal endothelial findings i ...... eterozygous mutations in KERA.
@en
Corneal endothelial findings i ...... eterozygous mutations in KERA.
@nl
P2860
P50
P1433
P1476
Corneal endothelial findings i ...... eterozygous mutations in KERA.
@en
P2093
Michalis Palos
P2860
P304
P356
10.3109/13816810.2013.811272
P577
2013-07-08T00:00:00Z