Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

JoAnn Bergoffen, S. S. Scherer, S. Wang et al. · Science · 1993 · 1.1K citations

Medicine, Genetics, Molecular Genetics +16

Defective myosin VIIA gene responsible for Usher syndrome type IB

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

Life Sciences, Genetics, Molecular Genetics +7

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

Mayada Tassabehji, Andrew Read, Valerie Newton et al. · Nature · 1992 · 694 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

Toshihiko Kikuchi, R. S. Kimura, DavidL. Paul et al. · Anatomy and Embryology · 1995 · 594 citations

Health Professions, Neurobiology, Neuroscience +16

Mutations of the<i>Connexin43</i>Gap-Junction Gene in Patients with Heart Malformations and Defects of Laterality

Scott Britz-Cunningham, Maithili M. Shah, Craig W. Zuppan et al. · New England Journal of Medicine · 1995 · 381 citations

Life Sciences, Genetics, Molecular Genetics +17