[Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome].

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 51, Issue 6, 2013, Pages 443-447

  Liu, Yan yan ^a   Bao, Xin hua ^b   Wang, Shuang ^b   Fu, N ^b   Liu, Xiao yan ^b   Song, Fu ying ^b   Yang, Yan ling ^b   Wu, Y ^b   Zhang, Yue hua ^b   Wu, Jian xin ^b   Jiang, Yu wu ^b   Qin, Jiong ^b   Wu, Xi ru ^b  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MARKER; GLUCOSE TRANSPORTER; GLUCOSE TRANSPORTER 1; SLC2A1 PROTEIN, HUMAN;

BRAIN; CARBOHYDRATE METABOLISM, INBORN ERRORS; CHILD; DEFICIENCY; ELECTROENCEPHALOGRAPHY; EPILEPSY; FEMALE; FOLLOW UP; GENETICS; HUMAN; INFANT; KETOGENIC DIET; MALE; MOVEMENT DISORDERS; MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PATHOLOGY; PRESCHOOL CHILD; RADIOGRAPHY;

BIOLOGICAL MARKERS; BRAIN; CARBOHYDRATE METABOLISM, INBORN ERRORS; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; ELECTROENCEPHALOGRAPHY; EPILEPSY; FEMALE; FOLLOW-UP STUDIES; GLUCOSE TRANSPORTER TYPE 1; HUMANS; INFANT; KETOGENIC DIET; MAGNETIC RESONANCE IMAGING; MALE; MONOSACCHARIDE TRANSPORT PROTEINS; MOVEMENT DISORDERS; MUTATION;

EID: 84895837410     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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