Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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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
Phaeochromocytoma
Lancet 366:665-675, Lenders,J.W.M.,et al, 2005
Hereditary Neuropathy with Liability to Pressure Palsies
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