We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleClinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.AuthorsSchatz P; Ponjavic V; Andréasson S; McGee TL; Dryja TP; Abrahamson MPublicationOphthalmic genetics, 2005, Vol 26, Issue 3, p119ISSN1381-6810Publication typearticleDOI10.1080/13816810500229090