Zobrazeno 1 - 4
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pro vyhledávání: '"Shoujin Kuang"'
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-4 (2020)
Abstract Background Neonatal thrombocytopenia is common in preterm and term neonates admitted to neonatal intensive care units. The etiology behind neonatal thrombocytopenia is complex. Inherited thrombocytopenia is rare and usually results from gene
Externí odkaz:
https://doaj.org/article/4aaa8f001bf74caca7f085cd5d4b1625
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-4 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background Neonatal thrombocytopenia is common in preterm and term neonates admitted to neonatal intensive care units. The etiology behind neonatal thrombocytopenia is complex. Inherited thrombocytopenia is rare and usually results from genetic mutat
Autor:
Yi Guo, Linyan Su, Jinsong Tang, Zuocheng Yang, Xiong Deng, Hao Deng, Ziqiang Luo, Shoujin Kuang, Jie Zhang, Jing Lei, Hongbo Xu
Publikováno v:
Psychiatric genetics. 22(6)
Variants of the BTB/POZ domain-containing protein 9 gene (BTBD9) (rs4714156, rs9357271, and rs9296249) and the serotonin 5-HT-2C receptor gene (HTR2C) (rs518147 and rs3813929) were reported to be associated with Tourette syndrome (TS) in White popula
Autor:
Shoujin Kuang, Linyan Su, Jie Zhang, Weidong Le, Hongbo Xu, Jinsong Tang, Joseph Jankovic, Yi Guo, Hao Deng, Zuocheng Yang, Xiong Deng
Publikováno v:
Neuroscience letters. 526(2)
Tourette syndrome (TS), a neurological disorder with a reported prevalence frequency ranging from 0.7% to 4.2%, is manifested by motor and phonic tics and associated with a variety of behavioral abnormalities including impulsivity. Clinical, neuroima