Human Genome Epidemiology Literature Finder
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Query Trace: CADASIL and TREX1[original query] |
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A homozygous NOTCH3 mutation p.R544C and a heterozygous TREX1 variant p.C99MfsX3 in a family with hereditary small vessel disease of the brain. Journal of the Chinese Medical Association : JCMA 2013 Jun 76 (6): 319-24. Soong Bing-Wen, Liao Yi-Chu, Tu Pang-Hsien, Tsai Pei-Chien, Lee I-Hui, Chung Chih-Ping, Lee Yi-Chu |
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- Page last updated:Apr 22, 2024
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