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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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2017 | 2 |
2021 | 1 |
2024 | 0 |
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Novel ALDH3A2 mutations in structural and functional domains of FALDH causing diverse clinical phenotypes in Sjögren-Larsson syndrome patients.
Hum Mutat. 2021 Aug;42(8):1015-1029. doi: 10.1002/humu.24236. Epub 2021 Jun 15.
Hum Mutat. 2021.
PMID: 34082469
3'-UTR SNP rs2229611 in G6PC1 affects mRNA stability, expression and Glycogen Storage Disease type-Ia risk.
Karthi S, Rajeshwari M, Francis A, Saravanan M, Varalakshmi P, Houlden H, Thangaraj K, Ashokkumar B.
Karthi S, et al. Among authors: rajeshwari m.
Clin Chim Acta. 2017 Aug;471:46-54. doi: 10.1016/j.cca.2017.05.016. Epub 2017 May 11.
Clin Chim Acta. 2017.
PMID: 28502559
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Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.
Udhayabanu T, Manole A, Rajeshwari M, Varalakshmi P, Houlden H, Ashokkumar B.
Udhayabanu T, et al. Among authors: rajeshwari m.
J Clin Med. 2017 May 5;6(5):52. doi: 10.3390/jcm6050052.
J Clin Med. 2017.
PMID: 28475111
Free PMC article.
Review.
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