Cost-effective molecular inversion probe-based ABCA4 sequencing reveals deep-intronic variants in Stargardt disease

Publication year

2019

Author(s)

Cremers, F.P.M.

Source

Human Mutation, 40, 10, (2019), pp. 1749-1759

ISSN

DOI

http://dx.doi.org/10.1002/humu.23787

Publication type

Article / Letter to editor

Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/208474

https://hdl.handle.net/2066/208474

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