Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Hepatitis and SLC25A13[original query] |
---|
Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations. Human mutation 2002 Feb 19 (2): 122-30. Yamaguchi Naoki, Kobayashi Keiko, Yasuda Tomotsugu, Nishi Ikumi, Iijima Mikio, Nakagawa Masanori, Osame Mitsuhiro, Kondo Ikuko, Saheki Takeyo |
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency. Journal of human genetics 2005 50 (7): 338-46. Lu Yao Bang, Kobayashi Keiko, Ushikai Miharu, Tabata Ayako, Iijima Mikio, Li Meng Xian, Lei Lei, Kawabe Kotaro, Taura Satoru, Yang Yanling, Liu Tze-Tze, Chiang Szu-Hui, Hsiao Kwang-Jen, Lau Yu-Lung, Tsui Lap-Chee, Lee Dong Hwan, Saheki Takeyo |
SLC25A13 gene mutations in Taiwanese patients with non-viral hepatocellular carcinoma. Molecular genetics and metabolism 2011 Jul 103 (3): 293-6. Chang Kuei-Wen, Chen Huey-Ling, Chien Yin-Hsiu, Chen Tse-Ching, Yeh Chau-Ti |
Neonatal intrahepatic cholestasis caused by citrin deficiency: prevalence and SLC25A13 mutations among Thai infants. BMC gastroenterology 2012 12 (1): 141. Treepongkaruna Suporn, Jitraruch Suttiruk, Kodcharin Porawee, Charoenpipop Dussadee, Suwannarat Pim, Pienvichit Paneeya, Kobayashi Keiko, Wattanasirichaigoon Duangrurd |
p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency. The Turkish journal of pediatrics 2018 1 59 (3): 311-314. ?eker-Y?lmaz Berna, Kör Deniz, Tümgör Gökhan, Ceylaner Serdar, Önenli-Mungan Neslih |
- Page last reviewed:Feb 1, 2024
- Content source: