Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease.
about
Novel compound heterozygous mutations in ABCA4 in a Chinese pedigree with Stargardt disease.Genetic analysis and clinical phenotype of two Indian families with X-linked choroideremia.Genotypic spectrum and phenotype correlations of ABCA4-associated disease in patients of south Asian descent.Genetic identification and molecular modeling characterization reveal a novel PROM1 mutation in Stargardt4-like macular dystrophy.Identification of a Novel Mutation in the ABCA4 Gene in a Chinese Family with Retinitis Pigmentosa Using Exome Sequencing.Possibilities for Using Pluripotent Stem Cells for Restoring Damaged Eye Retinal Pigment Epithelium
P2860
Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Identification of Novel Mutati ...... tients with Stargardt Disease.
@en
Identification of Novel Mutati ...... tients with Stargardt Disease.
@nl
type
label
Identification of Novel Mutati ...... tients with Stargardt Disease.
@en
Identification of Novel Mutati ...... tients with Stargardt Disease.
@nl
prefLabel
Identification of Novel Mutati ...... tients with Stargardt Disease.
@en
Identification of Novel Mutati ...... tients with Stargardt Disease.
@nl
P2093
P2860
P356
P1476
Identification of Novel Mutati ...... tients with Stargardt Disease.
@en
P2093
Anshuman Verma
Aparna Ganapathy
Govindasamy Kumaramanickavel
Jemima Jacob
Nallathambi Jeyabalan
Rajani Battu
Ramesh Hariharan
Ravi Kiran
Shuba Krishna
Vedam L Ramprasad
P2860
P304
P356
10.1155/2015/940864
P407
P577
2015-04-02T00:00:00Z