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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 2 |
2014 | 1 |
2024 | 0 |
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Page 1
De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood.
Nat Genet. 2013 Apr;45(4):445-9, 449e1. doi: 10.1038/ng.2562. Epub 2013 Feb 24.
Nat Genet. 2013.
PMID: 23435086
β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation.
Hayflick SJ, Kruer MC, Gregory A, Haack TB, Kurian MA, Houlden HH, Anderson J, Boddaert N, Sanford L, Harik SI, Dandu VH, Nardocci N, Zorzi G, Dunaway T, Tarnopolsky M, Skinner S, Holden KR, Frucht S, Hanspal E, Schrander-Stumpel C, Mignot C, Héron D, Saunders DE, Kaminska M, Lin JP, Lascelles K, Cuno SM, Meyer E, Garavaglia B, Bhatia K, de Silva R, Crisp S, Lunt P, Carey M, Hardy J, Meitinger T, Prokisch H, Hogarth P.
Hayflick SJ, et al.
Brain. 2013 Jun;136(Pt 6):1708-17. doi: 10.1093/brain/awt095. Epub 2013 May 17.
Brain. 2013.
PMID: 23687123
Free PMC article.
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A novel WDR45 mutation in a patient with static encephalopathy of childhood with neurodegeneration in adulthood (SENDA).
Ozawa T, Koide R, Nakata Y, Saitsu H, Matsumoto N, Takahashi K, Nakano I, Orimo S.
Ozawa T, et al.
Am J Med Genet A. 2014 Sep;164A(9):2388-90. doi: 10.1002/ajmg.a.36635. Epub 2014 Jul 10.
Am J Med Genet A. 2014.
PMID: 25044655
Free PMC article.
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