Anna M. Tracewska
ŁUKASIEWICZ Research Network PORT Polish Center For Technology Development
Wroclaw, DS 54066, Poland
Wroclaw, DS 54066, Poland
Last Updated: 09/26/2026
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Found 8 publications
Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis.
Journal: Frontiers in cell and developmental biology
Published: November 30, 2022
Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 28, 2021
Non-syndromic inherited retinal diseases in Poland: Genes, mutations, and phenotypes.
Journal: Molecular vision
Published: November 17, 2020
A Mild Phenotype Caused by Two Novel Compound Heterozygous Mutations in CEP290.
Journal: Genes
Published: September 17, 2020
DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 03, 2020
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 26, 2019
Genetic Spectrum of ABCA4-Associated Retinal Degeneration in Poland.
Journal: Genes
Published: October 22, 2019
Showing 1-8 of 8
Last Updated: 09/26/2026