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Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder | 501 |
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Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder | 16 | 32 | 16 | 24 | 32 | 19 | 11 |
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CaseReport_Whole Exome Sequencing.pdf | 294 |
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