Establishment of a non-integrated iPS cell line (SDQLCHi072-A) from a patient suffered from AUTS2 syndrome
Author:
Funder
Natural Science Foundation of Shandong Province
Publisher
Elsevier BV
Reference4 articles.
1. Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus;Beunders;Am. J. Hum. Genet.,2013
2. AUTS2 Syndrome: molecular mechanisms and model systems;Biel;Front. Mol. Neurosci.,2022
3. Attention deficit hyperactivity and autism spectrum disorders as the core symptoms of AUTS2 syndrome: description of five new patients and update of the frequency of manifestations and genotype-phenotype correlation;Sanchez-Jimeno;Genes (Basel),2021
4. Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins;Sultana;Genomics,2002
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