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Authors: Xue Zhong
Journal Article
Generation and characterization of a P2rx2 V60L mouse model for DFNA41 Free
Human Molecular Genetics, Volume 30, Issue 11, 1 June 2021, Pages 985–995, https://doi.org/10.1093/hmg/ddab077
Published: 31 March 2021
Journal Article
Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans Free
Human Molecular Genetics, Volume 28, Issue 3, 1 February 2019, Pages 515–523, https://doi.org/10.1093/hmg/ddy360
Published: 10 October 2018
Journal Article
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation Get access
Human Molecular Genetics, Volume 24, Issue 9, 1 May 2015, Pages 2482–2491, https://doi.org/10.1093/hmg/ddv009
Published: 18 January 2015
Journal Article
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism Get access
Human Molecular Genetics, Volume 17, Issue 15, 1 August 2008, Pages 2405–2415, https://doi.org/10.1093/hmg/ddn140
Published: 07 May 2008
Journal Article
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans Get access
Human Molecular Genetics, Volume 14, Issue 1, 1 January 2005, Pages 103–111, https://doi.org/10.1093/hmg/ddi010
Published: 10 November 2004
Journal Article
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss Get access
Human Molecular Genetics, Volume 12, Issue 10, 15 May 2003, Pages 1155–1162, https://doi.org/10.1093/hmg/ddg127
Published: 15 May 2003
Journal Article
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness Get access
Human Molecular Genetics, Volume 10, Issue 25, 1 December 2001, Pages 2945–2951, https://doi.org/10.1093/hmg/10.25.2945
Published: 01 December 2001
Journal Article
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss Get access
Human Molecular Genetics, Volume 9, Issue 1, 1 January 2000, Pages 63–67, https://doi.org/10.1093/hmg/9.1.63
Published: 01 January 2000
Journal Article
Myosin VIIA Gene: Heterogeneity of the Mutations Responsible for Usher Syndrome Type IB Get access
Human Molecular Genetics, Volume 6, Issue 1, January 1997, Pages 111–116, https://doi.org/10.1093/hmg/6.1.111
Published: 01 January 1997
Journal Article
The mutational spectrum in Waardenburg syndrome Get access
Human Molecular Genetics, Volume 4, Issue 11, November 1995, Pages 2131–2137, https://doi.org/10.1093/hmg/4.11.2131
Published: 01 November 1995
