Suchergebnisse - "Sun, Huihui"

PubPharm (6)

1

Analysis of parental origin of de novo SCN1A mutations in Dravet syndrome

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015

von Sun, H. | Zhang, Y. | Xu, X. | +2

2

Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations

enthalten in: Brain & development | 2014

von Xu, X. | Zhang, Y. | Sun, H. | +11

3

Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome

enthalten in: Journal of human genetics | 2010

von Sun, H. | Zhang, Y. | Liu, X. | +6

4

Gene symbol : SCN1A. Disease: Generalized epilepsy with febrile seizures plus

enthalten in: Human genetics | 2008

von Sun, H. | Zhang, Y. | Liang, J. | +7

5

Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy

enthalten in: Epilepsia | 2008

von Sun, H. | Zhang, Y. | Liang, J. | +5

6

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus

enthalten in: Journal of human genetics | 2008

von Sun, H. | Zhang, Y. | Liang, J. | +7

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