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Showing articles 0 to 6 of 6 Filter Applied: molecular genetics (Click to remove) Whipples Disease NEJM 356:55-66, Fenollar,F.,et al, 2007 Pediatric Leigh Syndrome Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020 Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing NEJM 370:Doi:10.1056/NEJMoal1401268, Wilson, M.R.,et al, 2014 The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene NEJM 354:2584-2592, Case 18-2006, 2006 Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992 Showing articles 0 to 6 of 6