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1998 | 1 |
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Page 1
Genetic characteristics of myoadenylate deaminase deficiency.
Ann Neurol. 1998 Jul;44(1):140-3. doi: 10.1002/ana.410440124.
Ann Neurol. 1998.
PMID: 9667605
Clinical Trial.
Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis.
Verrips A, Hoefsloot LH, Steenbergen GC, Theelen JP, Wevers RA, Gabreëls FJ, van Engelen BG, van den Heuvel LP.
Verrips A, et al. Among authors: steenbergen gc.
Brain. 2000 May;123 ( Pt 5):908-19. doi: 10.1093/brain/123.5.908.
Brain. 2000.
PMID: 10775536
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Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiency.
Schiller A, Wevers RA, Steenbergen GC, Blau N, Jung HH.
Schiller A, et al. Among authors: steenbergen gc.
Neurology. 2004 Oct 26;63(8):1524-6. doi: 10.1212/01.wnl.0000142083.47927.0a.
Neurology. 2004.
PMID: 15505183
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Molecular analysis of myophosphorylase deficiency in Dutch patients with McArdle's disease.
Martín MA, Rubio JC, Wevers RA, Van Engelen BG, Steenbergen GC, Van Diggelen OP, De Visser M, De Die-Smulders C, Blázquez A, Andreu AL, Arenas J.
Martín MA, et al. Among authors: steenbergen gc.
Ann Hum Genet. 2004 Jan;68(Pt 1):17-22. doi: 10.1046/j.1529-8817.2003.00067.x.
Ann Hum Genet. 2004.
PMID: 14748827
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