A novel GJB2 (connexin 26) mutation, F142L, in a patient with unusual mucocutaneous findings and deafness.
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G. Richard | C. Flaitz | P. Fang | S. Manolidis | B. Roa | Chester W Brown | H. Heilstedt | B. Reid | A. Hebert | Hsiao-Yuan Tang | R. Alford | M. Levy | K. Plunkett | M. Bender | Pil Chung | Chester W. Brown | P. Chung | Hsiao‐Yuan Tang