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Characterization of the Deleted in Autism 1 Protein Family: Implications for Studying Cognitive Disorders
Autism spectrum disorders (ASDs) are a group of commonly occurring, highly-heritable developmental disabilities. Human genes c3orf58 or Deleted In Autism-1 (DIA1) and cXorf36 or Deleted in Autism-1 Related (DIA1R) are implicated in ASD and mental retardation. Both gene products encode signal peptide...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023760/ https://www.ncbi.nlm.nih.gov/pubmed/21283809 http://dx.doi.org/10.1371/journal.pone.0014547 |