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Article

Are CSNK2A1 gene mutations associated with retinal dystrophy? Report of a patient carrier of a novel de novo splice site mutation.

Journal of human genetics - 1 Jun 2018

Colavito Davide, Del Giudice Elda, Ceccato Chiara, Dalle Carbonare Maurizio, Leon Alberta, Suppiej Agnese

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 29568000
DOI: 10.1038/s10038-018-0434-y

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