SCOPUS 정보 검색 플랫폼

Volumn 24, Issue 1, 2014, Pages 42-43

Screening of NLGN3 and NLGN4X genes in Thai children with autism spectrum disorder

(10) Mikhailov, Anna a Fennell, Alanna a Plong On, Oradawan c Sripo, Thanya c Hansakunachai, Tippawan d Roongpraiwan, Rawiwan e Sombuntham, Tasnawat e Ruangdaraganon, Nichara e Vincent, John B a,b Limprasert, Pornprot c

a CENTRE FOR ADDICTION AND MENTAL HEALTH (Canada)

b UNIVERSITY OF TORONTO (Canada)

c PRINCE OF SONGKLA UNIVERSITY (Thailand)

d THAMMASAT UNIVERSITY (Thailand)

e MAHIDOL UNIVERSITY (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; CODON; CODON USAGE; EXON; GENE; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; KARYOTYPING; LETTER; NLGN3 GENE; NLGN4X GENE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; THAILAND;

AUTISTIC DISORDER; CELL ADHESION MOLECULES, NEURONAL; CHILD, PRESCHOOL; FEMALE; HUMANS; MALE; MEMBRANE PROTEINS; NERVE TISSUE PROTEINS; THAILAND;

EID: 84891882894 PISSN: 09558829 EISSN: 14735873 Source Type: Journal
DOI: 10.1097/YPG.0000000000000019 Document Type: Letter

Times cited : (7)

References (5)

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2
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- A "silent" polymorphism in the MDR1 gene changes substrate specificity
- DOI 10.1126/science.1135308
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3
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- X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family
- DOI 10.1086/382137
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4
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5
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- Cell adhesion molecules and their involvement in autism spectrum disorder
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- Ye, H.¹ Liu, J.² Wu, J.Y.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.