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Volumn 18, Issue 4, 2015, Pages 233-236

Rett Syndrome as a Rare Disease: A European Perspective

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMMUNICATION SKILL; COMPARATIVE GENOMIC HYBRIDIZATION; EUROPEAN; GENE MUTATION; HEALTH CARE POLICY; HEALTH SERVICE; HUMAN; MEDICAL SOCIETY; MOLECULAR DIAGNOSIS; PRACTICE GUIDELINE; PRIORITY JOURNAL; PROFESSIONAL DEVELOPMENT; RARE DISEASE; RETT SYNDROME;

EID: 84937973332     PISSN: 16624246     EISSN: 16628063     Source Type: Journal    
DOI: 10.1159/000381139     Document Type: Article
Times cited : (2)

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  • 2
    • 84904465224 scopus 로고    scopus 로고
    • Genome sequencing identifies major causes of severe intellectual disability
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    • De novo mutations in human genetic disease
    • Veltman JA, Brunner HG: De novo mutations in human genetic disease. Nat Rev Genet 2012; 13: 565-575.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.