A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domain
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G. Vriend | C. Morton | H. Venselaar | U. Kim | L. Patthy | N. G. Robertson | B. Kang | M. Trexler | Hong‐Joon Park | Jeong‐In Baek | Kyu‐Yup Lee | Hyun-Ju Cho