Phenotypic variability associated with the D226N allele of IMPDH1.

Ali, Shahbaz

Phenotypic variability associated with the D226N allele of IMPDH1. [electronic resource] - Ophthalmology Feb 2015 - 429-31 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural

1549-4713

10.1016/j.ophtha.2014.07.057 doi


Adult
Aged
Alleles
Child
Consanguinity
Electroretinography
Female
Genetic Linkage
Humans
IMP Dehydrogenase--genetics
Infant
Male
Middle Aged
Pedigree
Phenotype
Photic Stimulation
Retinitis Pigmentosa--diagnosis
Young Adult