TY - GEN AU - Heathcote,K AU - Syrris,P AU - Carter,N D AU - Patton,M A TI - A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350) SN - 0022-2593 PY - 2000///0218 KW - Amino Acid Substitution KW - Connexin 26 KW - Connexins KW - genetics KW - Exons KW - Female KW - Hearing Loss, Sensorineural KW - Humans KW - Keratoderma, Palmoplantar KW - Male KW - Mutation, Missense KW - Pedigree KW - Polymorphism, Single-Stranded Conformational KW - Syndrome N1 - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't UR - https://doi.org/10.1136/jmg.37.1.50 ER -