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A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late‐onset non‐syndromic hearing loss in a Chinese family

S. Z. Yang, D. Yan, G. Feng, 2007, Clinical genetics.

Mutational spectrum in Usher syndrome type II

T. Balkany, S. Angeli, J. Hejtmancik, 2004, Clinical genetics.

USH1C: a rare cause of USH1 in a non‐Acadian population and a founder effect of the Acadian allele

T. Balkany, J. Hejtmancik, V. Newton, 2003, Clinical genetics.

Editorial :Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). DOI: 10.1080/15548627.2015.1100356;WOS:000373595400001; 2-s2.0-85013763791&;PMID: 26799652

Lee, Duchen, Izzo, 2016 .