No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins

Contactins and Contactin-Associated Proteins, and Contactin-Associated Protein-Like 2 (CNTNAP2) in particular, have been widely cited as autism risk genes based on findings from homozygosity mapping, molecular cytogenetics, copy number variation analyses, and both common and rare single nucleotide a...

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محفوظ في:
التفاصيل البيبلوغرافية
الحاوية / القاعدة:PLoS Genet
المؤلفون الرئيسيون: Murdoch, John D., Gupta, Abha R., Sanders, Stephan J., Walker, Michael F., Keaney, John, Fernandez, Thomas V., Murtha, Michael T., Anyanwu, Samuel, Ober, Gordon T., Raubeson, Melanie J., DiLullo, Nicholas M., Villa, Natalie, Waqar, Zainabdul, Sullivan, Catherine, Gonzalez, Luis, Willsey, A. Jeremy, Choe, So-Yeon, Neale, Benjamin M., Daly, Mark J., State, Matthew W.
التنسيق: Artigo
اللغة:Inglês
منشور في: Public Library of Science 2015
الموضوعات:
Research Article
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC4306541/
https://ncbi.nlm.nih.gov/pubmed/25621974
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1004852
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