Concepedia

A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24–25

Mirna Mustapha, Éliane Chouery, Delphine Torchard-Pagnez, Sylvie Nouaille, Awni Khrais, Fouad N. Sayegh, André Mégarbané, Jacques Loiselet, Mark Lathrop, Christine Petit,

Human Genetics · 2002 · 68 citations · 5 references

DOI

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References

5

Identification of EBP50: A PDZ-containing Phosphoprotein that Associates with Members of the Ezrin-Radixin-Moesin Family

David Reczek, Mark Berryman, Anthony Bretscher · The Journal of Cell Biology · 1997 · 589 citations · Full text

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Usher syndrome: An otoneurologic study

Claes G. Möller, Lars Ödkvist, William J. Kimberling et al. · The Laryngoscope · 1989 · 125 citations

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Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B.

Richard T. Libby, Karen P. Steel · PubMed · 2001 · 83 citations

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A New Locus for Late-Onset, Progressive, Hereditary Hearing Loss DFNA20 Maps to 17q25

Robert J. Morell, Karen H. Friderici, Sainan Wei et al. · Genomics · 2000 · 65 citations

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Vestibular Pathology in a New-mutant Mouse

Ken Kitamura, Masato Yagi, Yasuhiro Yoshikawa et al. · Acta Oto-Laryngologica · 1991 · 17 citations

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