First report of GLUT1 deficiency syndrome in Chinese patients with novel and hot spot mutations in SLC2A1 gene
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-02-01
著者
-
Wong Jack
School Of Biomedical Sciences Fac. Of Medicine The Chinese Univ. Of Hong Kong Shatin New Territories
-
Hui Joannie
Department Of Paediatrics Prince Of Wales Hospital The Chinese University Of Hong Kong Hong Kong Spe
-
Ng Tzi-bun
School Of Biomedical Sciences Faculty Of Medicine The Chinese University Of Hong Kong
-
Wong Jack
School Of Biomedical Sciences The Chinese University Of Hong Kong
-
Fung Eva
Department Of Paediatrics The Chinese University Of Hong Kong
-
HO Yuan
Genetics of Complex Disorders Training Program, Division of Statistical Genetics, Department of Bios
-
FONG Nga-Yin
School of Biomedical Sciences, The Chinese University of Hong Kong
-
KLEPPER Joerg
Department of Paediatrics and Paediatric Neurology, Children's Hospital
-
STEPHEN TSUI
School of Biomedical Sciences, The Chinese University of Hong Kong
-
Ho Yuan
Genetics Of Complex Disorders Training Program Division Of Statistical Genetics Department Of Biosta
-
Stephen Tsui
School Of Biomedical Sciences The Chinese University Of Hong Kong
-
Fong Nga-yin
School Of Biomedical Sciences The Chinese University Of Hong Kong
-
Klepper Joerg
Department Of Paediatrics And Paediatric Neurology Children's Hospital
-
Ng Tzi-bun
School Of Biomedical Sciences The Chinese University Of Hong Kong
-
Hui Joannie
Department Of Paediatrics The Chinese University Of Hong Kong
関連論文
- Thermostable Kunitz trypsin inhibitor with cytokine inducing, antitumor and HIV-1 reverse transcriptase inhibitory activities from Korean large black soybeans(ENZYMOLOGY, PROTEIN ENGINEERING, AND ENZYME TECHNOLOGY)
- Campesin, a thermostable antifungal peptide with highly potent antipathogenic activities(MISCELLANEOUS)
- Mutational and haplotype analysis of AGL in patients with glycogen storage disease type III
- Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese : Identification of 17 novel mutations and its genetic heterogeneity
- Galactorrhea : A strong clinical clue towards the diagnosis of neurotransmitter disease
- Purification and characterization of a novel serine protease from the mushroom Pholiota nameko(ENZYMOLOGY, PROTEIN ENGINEERING, AND ENZYME TECHNOLOGY)
- First report of GLUT1 deficiency syndrome in Chinese patients with novel and hot spot mutations in SLC2A1 gene
- Abnormal Leptin Bioavailability in Adolescent Idiopathic Scoliosis : An Important New Finding