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Year | Number of Results |
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2008 | 1 |
2010 | 1 |
2012 | 1 |
2024 | 0 |
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A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders.
Autism Res. 2008 Aug;1(4):251-7. doi: 10.1002/aur.30.
Autism Res. 2008.
PMID: 19360675
Free PMC article.
Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts.
Kruer MC, Paudel R, Wagoner W, Sanford L, Kara E, Gregory A, Foltynie T, Lees A, Bhatia K, Hardy J, Hayflick SJ, Houlden H.
Kruer MC, et al.
Neurosci Lett. 2012 Aug 8;523(1):35-8. doi: 10.1016/j.neulet.2012.06.036. Epub 2012 Jun 25.
Neurosci Lett. 2012.
PMID: 22743658
Free PMC article.
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Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease.
Dos Santos AV, Pestana CP, Diniz KR, Campos M, Abdalla-Carvalho CB, de Rosso AL, Pereira JS, Nicaretta DH, de Carvalho WL, Dos Santos JM, Santos-Rebouças CB, Pimentel MM.
Dos Santos AV, et al.
Neurosci Lett. 2010 Nov 19;485(2):121-4. doi: 10.1016/j.neulet.2010.08.083. Epub 2010 Sep 17.
Neurosci Lett. 2010.
PMID: 20816920
Free article.
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