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Complex I function in familial and sporadic dystonia.
Schapira AH, Warner T, Gash MT, Cleeter MW, Marinho CF, Cooper JM. Schapira AH, et al. Ann Neurol. 1997 Apr;41(4):556-9. doi: 10.1002/ana.410410421. Ann Neurol. 1997. PMID: 9124815
No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders.
Ahmad-Annuar A, Shah P, Hafezparast M, Hummerich H, Witherden AS, Morrison KE, Shaw PJ, Kirby J, Warner TT, Crosby A, Proukakis C, Wilkinson P, Orrell RW, Bradley L, Martin JE, Fisher EM. Ahmad-Annuar A, et al. Among authors: warner tt. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):150-7. doi: 10.1080/14660820310011737. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129801
238 results