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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1998 | 1 |
2009 | 1 |
2010 | 1 |
2018 | 1 |
2024 | 0 |
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Spectrum of PEX6 mutations in Zellweger syndrome spectrum patients.
Hum Mutat. 2010 Jan;31(1):E1058-70. doi: 10.1002/humu.21153.
Hum Mutat. 2010.
PMID: 19877282
Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
Yik WY, Steinberg SJ, Moser AB, Moser HW, Hacia JG.
Yik WY, et al.
Hum Mutat. 2009 Mar;30(3):E467-80. doi: 10.1002/humu.20932.
Hum Mutat. 2009.
PMID: 19105186
Free PMC article.
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Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders.
Chang CC, Gould SJ.
Chang CC, et al.
Am J Hum Genet. 1998 Nov;63(5):1294-306. doi: 10.1086/302103.
Am J Hum Genet. 1998.
PMID: 9792857
Free PMC article.
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Whole exome sequencing in neurogenetic odysseys: An effective, cost- and time-saving diagnostic approach.
Córdoba M, Rodriguez-Quiroga SA, Vega PA, Salinas V, Perez-Maturo J, Amartino H, Vásquez-Dusefante C, Medina N, González-Morón D, Kauffman MA.
Córdoba M, et al.
PLoS One. 2018 Feb 1;13(2):e0191228. doi: 10.1371/journal.pone.0191228. eCollection 2018.
PLoS One. 2018.
PMID: 29389947
Free PMC article.
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