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Test-SequenceVariant
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# proj.
# Ann.
updated_at
PubMed
15099351
Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia. Prop
1.09 KB
2015-11-18
12
5
2021-12-23
PubMed
24126708
Association of common genetic variants of HOMER1 gene with levodopa adverse effects in Parkinson's d
1.13 KB
2016-01-15
12
5
2021-12-23
PubMed
21699520
PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and
1.54 KB
2016-01-03
13
5
2021-12-23
PubMed
22180037
Genetic polymorphism of the glutathione-S-transferase P1 gene (GSTP1) and susceptibility to prostate
1.33 KB
2015-11-26
13
4
2021-12-23
PubMed
17318851
Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to
1.5 KB
2015-12-26
11
4
2021-12-23
PubMed
17327131
Molecular analysis of the CYP2F1 gene: identification of a frequent non-functional allelic variant.
1.71 KB
2015-12-28
12
4
2021-12-23
PubMed
17935240
Somatic and gonadal mosaicism in X-linked retinitis pigmentosa. The g.ORF15 + 652-653delAG mutation
1.55 KB
2015-11-23
11
4
2021-12-23
PubMed
17962394
Skewed X inactivation in an X linked nystagmus family resulted from a novel, p.R229G, missense mutat
1.3 KB
2015-11-23
13
4
2021-12-23
PubMed
15041272
A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation. Clinical, l
1.53 KB
2015-11-18
19
4
2021-12-23
PubMed
19521089
Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's d
978 Bytes
2015-08-06
9
4
2021-12-23
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