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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and SLC20A2[original query]
Novel mutations of PDGFRB cause primary familial brain calcification in Chinese families.
Journal of human genetics 2017 Mar .
Wang Chong, Yao Xiang-Ping, Chen Hai-Ting, Lai Jing-Hui, Guo Xin-Xin, Su Hui-Zhen, Dong En-Lin, Zhang Qi-Jie, Wang Ning, Chen Wan-J
Renal phosphate handling and inherited disorders of phosphate reabsorption: an update.
Pediatric nephrology (Berlin, Germany) 2017 12 34 (4): 549-559.
Wagner Carsten A, Rubio-Aliaga Isabel, Hernando Na
Identification of SLC20A2 deletions in patients with primary familial brain calcification.
Clinical genetics 2019 3 96 (1): 53-60.
Guo Xin-Xin, Su Hui-Zhen, Zou Xiao-Huan, Lai Lu-Lu, Lu Ying-Qian, Wang Chong, Li Yun-Lu, Hong Jing-Mei, Zhao Miao, Lin Kun-Xin, Lin Jie, Zeng Yi-Heng, Yao Xiang-Ping, Wang Ning, Chen Wan-J
Genomic Diagnoses for Ectopic Intracerebral Calcifications.
Neurology. Genetics 2023 8 9 (5): e200083.
Changrui Xiao, Thomas Cassini, Daniel Benavides, Anusha Ebrahim, David Adams, Camilo To
Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6.
Gene 2024 6 927 148731.
Clara Schott, Allison A Dilliott, Jian Wang, Adam D McIntyre, Surim Son, Samantha Colaiacovo, Cadence Baker, Lakshman Gunaratnam, Andrew A House, Shih-Han Susan Huang, Hariharan Iyer, John Johnson, Khaled Lotfy, Mario Masellis, Douglas P Munoz, Faisal Rehman, Pavel S Roshanov, Richard H Swartz, Matthew A Weir, Robert A Hegele, Dervla M Connaught
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