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Items where Author is "Banin, Eyal"

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Group by: Date | Item Type | Refereed
Jump to: 2021 | 2018
Number of items: 2.

2021

Ruberto, Francesco Paolo and Balzano, Sara and Namburi, Prasanthi and Kimchi, Adva and Pescini-Gobert, Rosanna and Obolensky, Alexey and Banin, Eyal and Ben-Yosef, Tamar and Sharon, Dror and Rivolta, Carlo. (2021) Heterozygous deletions of noncoding parts of the PRPF31 gene cause retinitis pigmentosa via reduced gene expression. Molecular Vision, 27. pp. 107-116.

2018

Khateb, Samer and Kowalewski, Björn and Bedoni, Nicola and Damme, Markus and Pollack, Netta and Saada, Ann and Obolensky, Alexey and Ben-Yosef, Tamar and Gross, Menachem and Dierks, Thomas and Banin, Eyal and Rivolta, Carlo and Sharon, Dror. (2018) A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans. Genetics in medicine, 20 (9). pp. 1004-1012.

This list was generated on Wed Apr 17 19:10:36 2024 CEST.