Association between FOXP2 gene and speech sound disorder in Chinese population

Psychiatry and Clinical Neurosciences

Volumn 64, Issue 5, 2010, Pages 565-573

  Zhao, Yunjing ^a   Ma, Hongwei ^a   Wang, Yueping ^b   Gao, Hong ^b   Xi, Chunyan ^a   Hua, Tainyi ^a   Zhao, Yaru ^a   Qiu, Guangrong ^a  

^a CHINA MEDICAL UNIVERSITY   (China)

^b Department of Urology   (China)

Author keywords

articulation disorder; DNA sequencing; FOXP2 gene; haplotype analysis; single nucleotide polymorphism

Indexed keywords

GLUTAMINE; TRANSCRIPTION FACTOR FOXP2;

AMINO ACID SEQUENCE; ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; EXON; FEMALE; GENETIC ASSOCIATION; GENETIC SCREENING; GENOTYPE; HAPLOTYPE; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SPEECH DISORDER; SPEECH SOUND DISORDER;

ALLELES; ARTICULATION DISORDERS; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CHINA; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; DNA; DNA PRIMERS; EXONS; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENOTYPE; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 77957369675     PISSN: 13231316     EISSN: 14401819     Source Type: Journal    
DOI: 10.1111/j.1440-1819.2010.02123.x     Document Type: Article

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