Analysis of the PRPF31 Gene in Spanish Autosomal Dominant Retinitis Pigmentosa Patients: A Novel Genomic Rearrangement.
about
Assessment of the incorporation of CNV surveillance into gene panel next-generation sequencing testing for inherited retinal diseases.Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathies.A new approach based on targeted pooled DNA sequencing identifies novel mutations in patients with Inherited Retinal Dystrophies
P2860
Analysis of the PRPF31 Gene in Spanish Autosomal Dominant Retinitis Pigmentosa Patients: A Novel Genomic Rearrangement.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
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
2017年论文
@zh
2017年论文
@zh-cn
name
Analysis of the PRPF31 Gene in ...... A Novel Genomic Rearrangement.
@en
type
label
Analysis of the PRPF31 Gene in ...... A Novel Genomic Rearrangement.
@en
prefLabel
Analysis of the PRPF31 Gene in ...... A Novel Genomic Rearrangement.
@en
P2093
P356
P1476
Analysis of the PRPF31 Gene in ...... A Novel Genomic Rearrangement.
@en
P2093
Almudena Avila-Fernandez
Berta Almoguera
Blanca Garcia-Sandoval
Fiona Blanco-Kelly
Inmaculada Martin-Merida
Luciana Rodriguez-Jacy da Silva
Maria Isabel Lopez-Molina
Miguel Carballo
Patricia Fernandez-San Jose
Raquel Perez-Carro
P304
P356
10.1167/IOVS.16-20515
P407
P577
2017-02-01T00:00:00Z