Next-generation sequencing-based comprehensive molecular analysis of 43 Japanese patients with cone and cone-rod dystrophies.
about
Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian FamiliesThe correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypes.CDHR1 mutations in retinal dystrophies.Clinical and genetic characteristics of 251 consecutive patients with macular and cone/cone-rod dystrophy.Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing.A novel CRX frameshift mutation causing cone-rod dystrophy in a Chinese family: A case report
P2860
Next-generation sequencing-based comprehensive molecular analysis of 43 Japanese patients with cone and cone-rod dystrophies.
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
Next-generation sequencing-bas ...... cone and cone-rod dystrophies.
@ast
Next-generation sequencing-bas ...... cone and cone-rod dystrophies.
@en
type
label
Next-generation sequencing-bas ...... cone and cone-rod dystrophies.
@ast
Next-generation sequencing-bas ...... cone and cone-rod dystrophies.
@en
prefLabel
Next-generation sequencing-bas ...... cone and cone-rod dystrophies.
@ast
Next-generation sequencing-bas ...... cone and cone-rod dystrophies.
@en
P2093
P2860
P1433
P1476
Next-generation sequencing-bas ...... cone and cone-rod dystrophies.
@en
P2093
Akio Oishi
Fumihiko Matsuda
Koichiro Higasa
Maho Oishi
Norimoto Gotoh
Satoshi Morooka
Yukiko Makiyama
P2860
P304
P577
2016-02-20T00:00:00Z