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Results: 1-25 | 26-28 |
Results: 26-28/28
Infantile encephalopathy associated with the MELAS A3243G mutation
Authors: Sue, CM Bruno, C Andreu, AL Cargan, A Mendell, JR Tsao, CY Luquette, M Paolicchi, J Shanske, S DiMauro, S De Vivo, DC
Citation: Cm. Sue et al., Infantile encephalopathy associated with the MELAS A3243G mutation, J PEDIAT, 134(6), 1999, pp. 696-700
Charcot-Marie-Tooth neuropathies and related disorders
Authors: Mendell, JR
Citation: Jr. Mendell, Charcot-Marie-Tooth neuropathies and related disorders, SEM NEUROL, 18(1), 1998, pp. 41-47
Intragenic telSMN mutations: Frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number
Authors: Parsons, DW McAndrew, PE Iannaccone, ST Mendell, JR Burghes, AHM Prior, TW
Citation: Dw. Parsons et al., Intragenic telSMN mutations: Frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number, AM J HU GEN, 63(6), 1998, pp. 1712-1723
Risultati: 1-25 | 26-28 |