De novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome
Torres, Alcy, Brownstein, Catherine A., Tembulkar, Sahil K., Graber, Kelsey, Genetti, Casie, Kleiman, Robin J., Sweadner, Kathleen J., Mavros, Chrystal, Liu, Kevin X., Smedemark-Margulies, Niklas, MasТом:
16
Мова:
english
Журнал:
Molecular Genetics and Metabolism Reports
DOI:
10.1016/j.ymgmr.2018.06.001
Date:
September, 2018
Файл:
PDF, 753 KB
english, 2018
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