Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1
Main Authors: | Rizel, Leah, Safieh, Christine, Shalev, Stavit A., Mezer, Eedy, Jabaly-Habib, Haneen, Ben-Neriah, Ziva, Chervinsky, Elena, Briscoe, Daniel, Ben-Yosef, Tamar |
---|---|
Format: | Online |
Language: | English |
Published: |
Molecular Vision
2011
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250379/ |
Similar Items
-
A novel splice site mutation of CDHR1 in a consanguineous Israeli Christian Arab family segregating autosomal recessive cone-rod dystrophy
by: Cohen, Ben, et al.
Published: (2012) -
MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome
by: Sodi, Andrea, et al.
Published: (2014) -
Genetic heterogeneity and consanguinity lead to a “double hit”: Homozygous mutations of MYO7A and PDE6B in a patient with retinitis pigmentosa
by: Goldenberg-Cohen, Nitza, et al.
Published: (2013) -
A Novel Frameshift Mutation of the USH2A Gene in a Korean Patient with Usher Syndrome Type II
by: Boo, Sung Hyun, et al.
Published: (2013) -
Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families
by: Huang, Xiu-Feng, et al.
Published: (2013)