Connexin Mutations and Hereditary Diseases
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DOI: 10.3390/ijms23084255
Abstract: Inherited diseases caused by connexin mutations are found in multiple organs and include hereditary deafness, congenital cataract, congenital heart diseases, hereditary skin diseases, and X-linked Charcot–Marie–Tooth disease (CMT1X). A large number of knockout and knock-in… read more here.
Keywords: function; pathology; mutations hereditary; cx32 ... See more keywords