TY  - GEN
AU  - Ali,Shahbaz
AU  - Khan,Shahid Y
AU  - Naeem,Muhammad Asif
AU  - Khan,Shaheen N
AU  - Husnain,Tayyab
AU  - Riazuddin,Saima
AU  - Ayyagari,Radha
AU  - Riazuddin,Sheikh
AU  - Hejtmancik,J Fielding
AU  - Riazuddin,S Amer
TI  - Phenotypic variability associated with the D226N allele of IMPDH1
SN  - 1549-4713
PY  - 2015///0414
KW  - Adult
KW  - Aged
KW  - Alleles
KW  - Child
KW  - Consanguinity
KW  - Electroretinography
KW  - Female
KW  - Genetic Linkage
KW  - Humans
KW  - IMP Dehydrogenase
KW  - genetics
KW  - Infant
KW  - Male
KW  - Middle Aged
KW  - Pedigree
KW  - Phenotype
KW  - Photic Stimulation
KW  - Retinitis Pigmentosa
KW  - diagnosis
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural
UR  - https://doi.org/10.1016/j.ophtha.2014.07.057
ER  -