HuGE Literature Finder
Records 1-3
Mutational and clinical spectrum in a cohort of Chinese patients with hereditary nemaline myopathy.
Clinical genetics 2020 Mar . Wang Qi, Hu Zhenxian, Chang Xingzhi, Yu Meng, Xie Zhiying, Lv He, Zhang Wei, Xiong Hui, Yuan Yun, Wang Zhaox |
Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population.
Clinical genetics 2016 May . Fattahi Zohreh, Kalhor Zahra, Fadaee Mahsa, Vazehan Raheleh, Parsimehr Elham, Abolhassani Ayda, Beheshtian Maryam, Zamani Gholamreza, Nafissi Shahriar, Nilipour Yalda, Akbari Mohammad R, Kahrizi Kimia, Kariminejad Ariana, Najmabadi Hosse |
Epigenetic and genetic variations at the TNNT1 gene locus are associated with HDL-C levels and coronary artery disease.
Epigenomics 2016 Mar . Guay Simon-Pierre, Légaré Cécilia, Brisson Diane, Mathieu Patrick, Bossé Yohan, Gaudet Daniel, Bouchard Lui |
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- Page last updated:Jan 19, 2021
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