TY  - GEN
AU  - Kabir,Firoz
AU  - Ullah,Inayat
AU  - Ali,Shahbaz
AU  - Gottsch,Alexander D H
AU  - Naeem,Muhammad Asif
AU  - Assir,Muhammad Zaman
AU  - Khan,Shaheen N
AU  - Akram,Javed
AU  - Riazuddin,Sheikh
AU  - Ayyagari,Radha
AU  - Hejtmancik,J Fielding
AU  - Riazuddin,S Amer
TI  - Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases
SN  - 1090-0535
PY  - 2018///0115
KW  - Base Sequence
KW  - Consanguinity
KW  - DNA Mutational Analysis
KW  - Electroretinography
KW  - Exons
KW  - Eye Proteins
KW  - genetics
KW  - Female
KW  - Genetic Linkage
KW  - Genome-Wide Association Study
KW  - Humans
KW  - Lod Score
KW  - Loss of Function Mutation
KW  - Male
KW  - Microtubule-Associated Proteins
KW  - Mutation
KW  - Pedigree
KW  - Polymerase Chain Reaction
KW  - Retinitis Pigmentosa
KW  - diagnosis
KW  - Young Adult
N1  - Publication Type: Journal Article
ER  -