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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 2 |
2013 | 3 |
2024 | 0 |
PubMed for id: 599046675
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Page 1
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy.
PLoS One. 2013 Dec 16;8(12):e82154. doi: 10.1371/journal.pone.0082154. eCollection 2013.
PLoS One. 2013.
PMID: 24358150
Free PMC article.
Combined analysis of circulating β-endorphin with gene polymorphisms in OPRM1, CACNAD2 and ABCB1 reveals correlation with pain, opioid sensitivity and opioid-related side effects.
Rhodin A, Grönbladh A, Ginya H, Nilsson KW, Rosenblad A, Zhou Q, Enlund M, Hallberg M, Gordh T, Nyberg F.
Rhodin A, et al.
Mol Brain. 2013 Feb 12;6:8. doi: 10.1186/1756-6606-6-8.
Mol Brain. 2013.
PMID: 23402298
Free PMC article.
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Early infantile epileptic encephalopathy associated with a high voltage gated calcium channelopathy.
Edvardson S, Oz S, Abulhijaa FA, Taher FB, Shaag A, Zenvirt S, Dascal N, Elpeleg O.
Edvardson S, et al.
J Med Genet. 2013 Feb;50(2):118-23. doi: 10.1136/jmedgenet-2012-101223.
J Med Genet. 2013.
PMID: 23339110
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The 630-kb lung cancer homozygous deletion region on human chromosome 3p21.3: identification and evaluation of the resident candidate tumor suppressor genes. The International Lung Cancer Chromosome 3p21.3 Tumor Suppressor Gene Consortium.
Lerman MI, Minna JD.
Lerman MI, et al.
Cancer Res. 2000 Nov 1;60(21):6116-33.
Cancer Res. 2000.
PMID: 11085536
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Functional properties of a new voltage-dependent calcium channel alpha(2)delta auxiliary subunit gene (CACNA2D2).
Gao B, Sekido Y, Maximov A, Saad M, Forgacs E, Latif F, Wei MH, Lerman M, Lee JH, Perez-Reyes E, Bezprozvanny I, Minna JD.
Gao B, et al.
J Biol Chem. 2000 Apr 21;275(16):12237-42. doi: 10.1074/jbc.275.16.12237.
J Biol Chem. 2000.
PMID: 10766861
Free PMC article.
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