SCOPUS 정보 검색 플랫폼

Volumn 45, Issue 1, 2011, Pages 49-53

A novel GPR56 mutation causes bilateral frontoparietal polymicrogyria

(8) Luo, Rong a Yang, Hye Min a Jin, Zhaohui a Halley, Dicky J J b Chang, Bernard S c MacPherson, Lesley d Brueton, Louise e Piao, Xianhua a

a BOSTON CHILDREN S HOSPITAL (United States)

b ERASMUS MEDICAL CENTER (Netherlands)

c HARVARD MEDICAL SCHOOL (United States)

d BIRMINGHAM CHILDREN S HOSPITAL (United Kingdom)

e BIRMINGHAM WOMEN S HOSPITAL (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CELL SURFACE PROTEIN; G PROTEIN COUPLED RECEPTOR; VALPROIC ACID;

AMINO TERMINAL SEQUENCE; ANAMNESIS; ARTICLE; BILATERAL FRONTOPARIETAL POLYMICROGYRIA; CARBOXY TERMINAL SEQUENCE; CASE REPORT; CELL CULTURE; CELL SURFACE; CHEMICAL ANALYSIS; CHILD; CONSANGUINITY; CONVERGENT STRABISMUS; GENE; GENE EXPRESSION; GENETIC TRANSFECTION; GPR56 GENE; GROWTH RETARDATION; HEAD CIRCUMFERENCE; HUMAN; MALE; MICROGYRIA; MISSENSE MUTATION; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PALPEBRAL FISSURE ANOMALY; PEDIGREE; PRIORITY JOURNAL; PROTEIN DEGRADATION; SEIZURE; SEQUENCE ANALYSIS; WESTERN BLOTTING;

CHILD, PRESCHOOL; FRONTAL LOBE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MALFORMATIONS OF CORTICAL DEVELOPMENT; MUTATION; NERVOUS SYSTEM MALFORMATIONS; PARIETAL LOBE; RECEPTORS, G-PROTEIN-COUPLED;

EID: 79959972979 PISSN: 08878994 EISSN: 18735150 Source Type: Journal
DOI: 10.1016/j.pediatrneurol.2011.02.004 Document Type: Article

Times cited : (24)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.