Genetic causes of syndromic and non-syndromic autism
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, cilt.52, sa.2, ss.130-138, 2010 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Derleme
- Cilt numarası: 52 Sayı: 2
- Basım Tarihi: 2010
- Doi Numarası: 10.1111/j.1469-8749.2009.03523.x
- Dergi Adı: DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.130-138
- Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
- Dokuz Eylül Üniversitesi Adresli: Hayır
Özet
AIMS Over the past decade, genetic tests have become available for numerous heritable disorders, especially those whose inheritance follows the Mendelian model. Autism spectrum disorders (ASDs) represent a group of developmental disorders with a strong genetic basis. During the past few years, genetic research in ASDs has been successful in identifying several vulnerability loci and a few cytogenetic abnormalities or single-base mutations implicated in the causation of autism.