Mutations in the myosin VIAA gene cause a wide phenotypic spectrum, including atypical usher syndrome [5]

Xue Z Liu, C. Hope, J. Walsh, V. Newton, Mei Ke Xiao Mei Ke, Yu Liang Chuan Yu Liang, Ron Xu Li Ron Xu, Mu Zhou Jiu Mu Zhou, D. Trump, K. P. Steel, S. Bundey, S. D M Brown

Research output: Contribution to journalArticle

87 Citations (Scopus)
Original languageEnglish
Pages (from-to)909-912
Number of pages4
JournalAmerican Journal of Human Genetics
Volume63
Issue number3
DOIs
StatePublished - Dec 1 1998
Externally publishedYes

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Usher Syndromes
Retinitis Pigmentosa
Deafness
Pedigree
Myosins
Phenotype
Mutation
Genes

ASJC Scopus subject areas

  • Genetics

Cite this

Liu, X. Z., Hope, C., Walsh, J., Newton, V., Xiao Mei Ke, M. K., Chuan Yu Liang, Y. L., ... Brown, S. D. M. (1998). Mutations in the myosin VIAA gene cause a wide phenotypic spectrum, including atypical usher syndrome [5]. American Journal of Human Genetics, 63(3), 909-912. https://doi.org/10.1086/302026

Mutations in the myosin VIAA gene cause a wide phenotypic spectrum, including atypical usher syndrome [5]. / Liu, Xue Z; Hope, C.; Walsh, J.; Newton, V.; Xiao Mei Ke, Mei Ke; Chuan Yu Liang, Yu Liang; Li Ron Xu, Ron Xu; Jiu Mu Zhou, Mu Zhou; Trump, D.; Steel, K. P.; Bundey, S.; Brown, S. D M.

In: American Journal of Human Genetics, Vol. 63, No. 3, 01.12.1998, p. 909-912.

Research output: Contribution to journalArticle

Liu, XZ, Hope, C, Walsh, J, Newton, V, Xiao Mei Ke, MK, Chuan Yu Liang, YL, Li Ron Xu, RX, Jiu Mu Zhou, MZ, Trump, D, Steel, KP, Bundey, S & Brown, SDM 1998, 'Mutations in the myosin VIAA gene cause a wide phenotypic spectrum, including atypical usher syndrome [5]', American Journal of Human Genetics, vol. 63, no. 3, pp. 909-912. https://doi.org/10.1086/302026
Liu, Xue Z ; Hope, C. ; Walsh, J. ; Newton, V. ; Xiao Mei Ke, Mei Ke ; Chuan Yu Liang, Yu Liang ; Li Ron Xu, Ron Xu ; Jiu Mu Zhou, Mu Zhou ; Trump, D. ; Steel, K. P. ; Bundey, S. ; Brown, S. D M. / Mutations in the myosin VIAA gene cause a wide phenotypic spectrum, including atypical usher syndrome [5]. In: American Journal of Human Genetics. 1998 ; Vol. 63, No. 3. pp. 909-912.
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