Associated Papers
Genetics of non-syndromic and syndromic oculocutaneous albinism in human and mouse.
Fernández A et al.
Pigment Cell & Melanoma Research, 2021
Prevalence and causes of infantile nystagmus in a large population-based Danish cohort.
Hvid K et al.
Acta Ophthalmologica, 2020
Molecular basis of the extreme dilution mottled mouse mutation: a combination of coding and noncoding genomic alterations.
Lavado A et al.
The Journal of Biological Chemistry, 2005
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