A family with autosomal dominant mutilating neuropathy not linked to either Charcot–Marie–Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci
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P. Girlanda | A. Pizzuti | E. Bellone | P. Mandich | A. Mazzeo | C. Rodolico | A. Toscano | D. Cassandrini | G. Vita | E. D. Maria | F. Ajmar | S. Pigullo | V. Macaione | E. Maria