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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 1 |
2022 | 1 |
2023 | 0 |
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2 results
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Page 1
Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits.
Genes (Basel). 2022 Feb 25;13(3):429. doi: 10.3390/genes13030429.
Genes (Basel). 2022.
PMID: 35327983
Free PMC article.
Comparison of three clinical rating scales in Friedreich ataxia (FRDA).
Bürk K, Mälzig U, Wolf S, Heck S, Dimitriadis K, Schmitz-Hübsch T, Hering S, Lindig TM, Haug V, Timmann D, Degen I, Kruse B, Dörr JM, Ratzka S, Ivo A, Schöls L, Boesch S, Klockgether T, Klopstock T, Schulz JB.
Bürk K, et al. Among authors: ivo a.
Mov Disord. 2009 Sep 15;24(12):1779-84. doi: 10.1002/mds.22660.
Mov Disord. 2009.
PMID: 19562766
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