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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 14, 2024. (Total: 232476Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Sleep Disorders and ASMT[original query]
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability.
BMC medical genetics 2011 1 12 17.
Pagan Cecile, Botros Hany Goubran, Poirier Karine, Dumaine Anne, Jamain Stéphane, Moreno Sarah, de Brouwer Arjan, Van Esch Hilde, Delorme Richard, Launay Jean-Marie, Tzschach Andreas, Kalscheuer Vera, Lacombe Didier, Briault Sylvain, Laumonnier Frédéric, Raynaud Martine, van Bon Bregje W, Willemsen Marjolein H, Leboyer Marion, Chelly Jamel, Bourgeron Thom
Genetic variation in melatonin pathway enzymes in children with autism spectrum disorder and comorbid sleep onset delay.
Journal of autism and developmental disorders 2015 Jan 45 (1): 100-10.
Veatch Olivia J, Pendergast Julie S, Allen Melissa J, Leu Roberta M, Johnson Carl Hirschie, Elsea Sarah H, Malow Beth
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