Aland eye disease: no albino misrouting

scientific article published in December 1985

Aland eye disease: no albino misrouting is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/J.1399-0004.1985.TB00421.X
P698PubMed publication ID4075563

P2093author name stringA W Eriksson
H Collewijn
A G van Vliet
J W Delleman
A T van Balen
D B van Dorp
H R Forsius
P433issue6
P921main subjectalbinismQ81867
eye diseaseQ3041498
P304page(s)526-531
P577publication date1985-12-01
P1433published inClinical GeneticsQ5133760
P1476titleAland eye disease: no albino misrouting
P478volume28

Reverse relations

cites work (P2860)
Q35016967A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype
Q35629094A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family
Q37312045Aland island eye disease: clinical and electrophysiological studies of a Welsh family
Q37560461Clinical Characteristics, Mutation Spectrum, and Prevalence of Åland Eye Disease/Incomplete Congenital Stationary Night Blindness in Denmark.
Q33596132Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.
Q35195904Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis.
Q35716618Molecular genetics of inherited retinal degenerations
Q88017490Retinal findings in a patient of French ancestry with CABP4-related retinal disease
Q34211524Vision in albinism

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