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Volumn 92, Issue 4, 2007, Pages 359-363

An Alu-mediated rearrangement causing a 3.2 kb deletion and a novel two base pair deletion in AAAS gene as the cause of triple A syndrome

Author keywords

AAAS gene; Alu mediated deletion; Triple A syndrome

Indexed keywords

ACHALASIA ADRENAL INSUFFICIENCY ALACRIMA SYNDROME GENE; ALLGROVE SYNDROME; ALU SEQUENCE; ARTICLE; BASE PAIRING; CASE REPORT; DNA FLANKING REGION; EXON; FEMALE; GENE; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INTRON; PRIORITY JOURNAL; SCHOOL CHILD; WILD TYPE;

EID: 36148953591     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2007.08.116     Document Type: Article
Times cited : (11)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.