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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
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2003 1
2004 1
2007 1
2009 1
2011 1
2012 2
2013 1
2014 2
2015 1
2016 1
2017 2
2018 2
2019 2
2020 3
2021 7
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2023 2
2024 0

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PubMed for id: 133686

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Page 1
Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant.
Pomerantz DJ, Ferdinandusse S, Cogan J, Cooper DN, Reimschisel T, Robertson A, Bican A, McGregor T, Gauthier J, Millington DS, Andrae JLW, Tschannen MR, Helbling DC, Demos WM, Denis S, Wanders RJA, Newman JN, Hamid R, Phillips JA 3rd; Collaborators of UDN. Pomerantz DJ, et al. Am J Med Genet A. 2018 Mar;176(3):692-698. doi: 10.1002/ajmg.a.38602. Epub 2018 Feb 1. Am J Med Genet A. 2018. PMID: 29388319 Free PMC article. Review.
35 results