Deletion of 16q24.1 supports a role for the ATP2C2 gene in specific language impairment

Journal of Child Neurology

Volumn 30, Issue 4, 2015, Pages 517-521

  Smith, Amena W ^a   Holden, Kenton R ^a,b   Dwivedi, Alka ^b   Dupont, Barbara R ^b   Lyons, Michael J ^b  

^a MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

^b GREENWOOD GENETIC CENTER   (United States)

Author keywords

ATP2C2; deletion; language delay; specific language impairment

Indexed keywords

ACADEMIC ACHIEVEMENT; ARTICLE; ATP2C2 GENE; CASE REPORT; CHILD; CHROMOSOME 16Q; CHROMOSOME DELETION; COMPREHENSION; DYSLEXIA; GENE; HUMAN; LANGUAGE DELAY; LANGUAGE DISABILITY; MALE; MICROARRAY ANALYSIS; MICROARRAY KIT; NARRATIVE; NERVE CELL DIFFERENTIATION; PHONETICS; PHYSICAL EXAMINATION; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIMARY SCHOOL; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; SCHOOL CHILD; SEMANTICS; SPEECH DELAY; SPEECH THERAPY; CHROMOSOME 16; GENETICS; LANGUAGE TEST;

ADENOSINE TRIPHOSPHATASE (CALCIUM); ATP2C2 PROTEIN, HUMAN;

CALCIUM-TRANSPORTING ATPASES; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; HUMANS; LANGUAGE DISORDERS; LANGUAGE TESTS; MALE; MICROARRAY ANALYSIS;

EID: 84923322818     PISSN: 08830738     EISSN: 17088283     Source Type: Journal    
DOI: 10.1177/0883073814545113     Document Type: Article

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