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Journal of Human Genetics|January 24, 2009
HLA-DPB1 and NFKBIL1 may confer the susceptibility to chronic thromboembolic pulmonary hypertension in the absence of deep vein thrombosisSatoshi Kominami, Nobuhiro Tanabe, Masao Ota, et al.Journal of Human Genetics|October 6, 2005
Identification and functional analysis of cystathionine beta-synthase gene mutations in patients with homocystinuriaSook-Jin Lee, Dong Hwan Lee, Han-Wook Yoo, et al.Journal of Human Genetics|October 6, 2005
Systematic classification of alleles of the glycophorin A (MN blood group) geneHajime Mizukami, Atsushi Akane, Nori Nakayashiki, et al.Journal of Human Genetics|September 13, 2005
G6PD Viangchan (871G>A) is the most common G6PD-deficient variant in the Cambodian populationChalisa Louicharoen, Issarang NuchprayoonJournal of Human Genetics|March 26, 2004
Novel mutations of EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformisGenshu Tate, Takao Suzuki, Koji Kishimoto, et al.Journal of Human Genetics|March 26, 2004
Catalog of 300 SNPs in 23 genes encoding G-protein coupled receptorsAritoshi Iida, Susumu Saito, Akihiro Sekine, et al.Journal of Human Genetics|September 1, 2004
Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndromeDong-Jik Shin, Yangsoo Jang, Hyun-Young Park, et al.Journal of Human Genetics|September 16, 2004
SMARCA2 and THAP11: potential candidates for polyglutamine disorders as evidenced from polymorphism and protein-folding simulation studiesNeeraj Pandey, Uma Mittal, Achal K Srivastava, et al.Journal of Human Genetics|September 16, 2004
Association of paraoxonase 1 gene polymorphisms with risk of Parkinson's disease: a meta-analysisElias Zintzaras, Georgios M HadjigeorgiouJournal of Human Genetics|August 2, 2005
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiencyYao Bang Lu, Keiko Kobayashi, Miharu Ushikai, et al.Pageof 353