Autosomal dominant retinitis pigmentosa with incomplete penetrance due to an intronic mutation of the PRPF31 gene

Tahleel Ali-Nasser, Shiri Zayit-Soudry, Eyal Banin, Dror Sharon, Tamar Ben-Yosef*

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

4 Scopus citations

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Keyphrases

Biochemistry, Genetics and Molecular Biology

Medicine and Dentistry

Immunology and Microbiology