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American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 114, Issue 2, 2002, Pages 137-143

Mutation screening and transmission disequilibrium study of ATP10C in autism

(9) Kim, Soo Jeong a Herzing, Laura B K a Veenstra VanderWeele, Jeremy c Lord, Catherine b Courchesne, Rachel a Leventhal, Bennett L d Ledbetter, David H e Courchesne, Eric a Cook Jr , Edwin H a

a UNIVERSITY OF CHICAGO (United States)

b Developmental Disorders Clinic Child and Adolescent Psychiatry (United States)

c Department of Psychiatry MC3077 ^* (United States)

d RADY CHILDREN'S HOSPITAL (United States)

e UNIVERSITY OF CALIFORNIA (United States)

Author keywords

15q11 q13; Association; ATP10C; Autism; Polymorphism

Indexed keywords

AMINOPHOSPHOLIPID; CARRIER PROTEIN; MEMBRANE PROTEIN;

ADULT; AGED; ARTICLE; AUTISM; BRAIN; CELL MEMBRANE; CHROMOSOME 15Q; DNA FLANKING REGION; FEMALE; FIBROBLAST; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC POLYMORPHISM; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN LOCALIZATION;

ADENOSINE TRIPHOSPHATASES; AUTISTIC DISORDER; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; INFANT; LINKAGE DISEQUILIBRIUM; MALE; MEMBRANE TRANSPORT PROTEINS; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 0037040481 PISSN: 15524841 EISSN: 1552485X Source Type: Journal
DOI: 10.1002/ajmg.10238 Document Type: Article

Times cited : (25)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.