scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1399-0004.1985.TB00421.X |
P698 | PubMed publication ID | 4075563 |
P2093 | author name string | A W Eriksson | |
H Collewijn | |||
A G van Vliet | |||
J W Delleman | |||
A T van Balen | |||
D B van Dorp | |||
H R Forsius | |||
P433 | issue | 6 | |
P921 | main subject | albinism | Q81867 |
eye disease | Q3041498 | ||
P304 | page(s) | 526-531 | |
P577 | publication date | 1985-12-01 | |
P1433 | published in | Clinical Genetics | Q5133760 |
P1476 | title | Aland eye disease: no albino misrouting | |
P478 | volume | 28 |
Q35016967 | A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype |
Q35629094 | A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family |
Q37312045 | Aland island eye disease: clinical and electrophysiological studies of a Welsh family |
Q37560461 | Clinical Characteristics, Mutation Spectrum, and Prevalence of Åland Eye Disease/Incomplete Congenital Stationary Night Blindness in Denmark. |
Q33596132 | Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome. |
Q35195904 | Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis. |
Q35716618 | Molecular genetics of inherited retinal degenerations |
Q88017490 | Retinal findings in a patient of French ancestry with CABP4-related retinal disease |
Q34211524 | Vision in albinism |
Search more.