Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 [Crumbs homologue 1] Mutations in Iranian Retinal Degeneration Families

Mohammad, Ghofrani; Mahin, Yahyaei; Man G., Brunner; Frans P.M., Cremers; Morteza, Movasat; Muhammad Imran, Khan; Mohammad, Keramatipour

Mohammad, Ghofrani; Mahin, Yahyaei; Man G., Brunner; Frans P.M., Cremers; Morteza, Movasat; Muhammad Imran, Khan; Mohammad, Keramatipour.

IBJ-Iranian Biomedical Journal. 2017; 21 (5): 294-302

in En | IMEMR | ID: emr-188486

Responsible library: EMRO

Subject(s)

Humans; Mutation; Retinitis Pigmentosa/genetics; Leber Congenital Amaurosis/genetics; Chromosome Mapping; Whole Genome Sequencing; Eye Proteins; Membrane Proteins; Nerve Tissue Proteins; Homozygote

Search on Google

Add to My VHL

XML

Index: IMEMR Main subject: Retinitis Pigmentosa / Chromosome Mapping / Eye Proteins / Leber Congenital Amaurosis / Whole Genome Sequencing / Homozygote / Membrane Proteins / Mutation / Nerve Tissue Proteins Limits: Humans Language: En Journal: Iran. Biomed. J. Year: 2017

Search on Google

Add to My VHL

XML