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25. R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease? López-Bigas N; Rabionet R; Arbonés ML; Estivill X Eur J Hum Genet; 2001 Jan; 9(1):70. PubMed ID: 11175305 [No Abstract] [Full Text] [Related]
26. Deafness-associated mutation opens the gate to understanding. Sedwick C J Gen Physiol; 2018 May; 150(5):647. PubMed ID: 29685927 [TBL] [Abstract][Full Text] [Related]
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