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Clinical spectrum in multiple families with primary COQ 10 deficiency.

Autor: Hashemi SS; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Zare-Abdollahi D; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Bakhshandeh MK; Department of Pediatrics, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran., Vafaee A; Department of Orthopedics, Tehran University of Medical Sciences, Tehran, Iran., Abolhasani S; Department of Neurology, Tabriz University of Medical Sciences, Tabriz, Iran., Inanloo Rahatloo K; School of Biology, College of Science, University of Tehran, Tehran, Iran., DanaeeFard F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Farboodi N; UCLA School of Public Health, Los Angeles, California, USA., Rohani M; Department of Neurology, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran., Alavi A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2021 Feb; Vol. 185 (2), pp. 440-452. Date of Electronic Publication: 2020 Nov 20.