Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders - Concepedia

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Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

77

Citations

27

References

2013

Year

J. J. T. van Harssel, Sarah Weckhuysen, Marjan J. A. van Kempen, Katia Hardies, Nienke E. Verbeek, Carolien G. F. de Kovel, W. Boudewijn Gunning, Emma van Daalen, Maretha Jonge, Anna Jansen,

Pcdh19-related Epilepsy SyndromesMendelian DisorderAutism Spectrum DisordersSyndromic AutismGeneticsGenetic DisorderAutismPcdh19 MutationsNeurologyMedicineNeurogenetics

References

	Year	Citations

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