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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 16, 2024. (Total: 231503Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Syndrome and GFPT1[original query]
Congenital myasthenic syndrome in Israel: Genetic and clinical characterization.
Neuromuscular disorders : NMD 2016 12 27 (2): 136-140.
Aharoni Sharon, Sadeh Menachem, Shapira Yehuda, Edvardson Simon, Daana Muhannad, Dor-Wollman Talia, Mimouni-Bloch Aviva, Halevy Ayelet, Cohen Rony, Sagie Liora, Argov Zohar, Rabie Malcolm, Spiegel Ronen, Chervinsky Ilana, Orenstein Naama, Engel Andrew G, Nevo Yor
Congenital Myasthenic Syndrome: Spectrum of Mutations in an Indian Cohort.
Journal of clinical neuromuscular disease 2018 Sep 20 (1): 14-27.
Selvam Pavalan, Arunachal Gautham, Danda Sumita, Chapla Aaron, Sivadasan Ajith, Alexander Mathew, Thomas Maya Mary, Thomas Nihal
Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis.
Pain 2021 Feb .
Suri Pradeep, Stanaway Ian B, Zhang Yanfei, Freidin Maxim B, Tsepilov Yakov A, Carrell David S, Williams Frances M K, Aulchenko Yurii S, Hakonarson Hakon, Namjou Bahram, Crosslin David R, Jarvik Gail P, Lee Ming
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