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2022
Mark A novel phenotype associated with the R162W variant in the KCNJ13 gene
Schroeder, Marion ^LU ; Peter, Virginie G. ; Gränse, Lotta ^LU ; Andréasson, Sten ^LU ; Rivolta, Carlo and Kjellström, Ulrika ^LU (2022) In Ophthalmic Genetics 43(4). p.500-507
- Contribution to journal › Article
1997
Mark Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
Ponjavic, Vesna ^LU (1997)
- Thesis › Doctoral thesis (compilation)