Concepedia

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

Salvatore Melchionda, Nadav Ahituv, Luigi Bisceglia, Tama Sobe, Fabian Glaser, Raquel Rabionet, María L. Arbonés, Angelo Notarangelo, Enzo Di Iorio, Massimo Carella,

The American Journal of Human Genetics · 2001 · 244 citations · 19 references

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19

Three-dimensional structure of myosin subfragment-1: a molecular motor

Ivan Rayment, W. Rypniewski, Karen Schmidt‐Bäse et al. · Science · 1993 · 2.1K citations

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Structure of the actin-myosin complex and its implications for muscle contraction

Ivan Rayment, Hazel M. Holden, Michael Whittaker et al. · Science · 1993 · 1.8K citations

, , +17

Defective myosin VIIA gene responsible for Usher syndrome type IB

Dominique Well, Stéphane Blanchard, Josseline Kaplan et al. · Nature · 1995 · 1.1K citations

, , +7

KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness

Christian Kubisch, Björn C. Schroeder, Thomas Friedrich et al. · Cell · 1999 · 868 citations · Full text

, , +17

A type VII myosin encoded by the mouse deafness gene shaker-1

Faith Gibson, James Walsh, Philomena Mburu et al. · Nature · 1995 · 682 citations

, , +10