Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language impairment

Overview of attention for article published in BMC Medical Genomics, February 2016

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PubMed: Characterisation of CASPR2 deficiency disorder--a syndrome involving autism, epilepsy and language… https://t.co/MuH6k3ionh

Speaking of @BMC_series, have you seen our paper on homozygous CNTNAP2 (CASPR2) mutations in patients? #autism https://t.co/twPBsH9ohi

PubMed: Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language… https://t.co/CJGzvtVAsm

RT @Genes_Speak: New paper from @Sonja_Vernes group in BMC Medical Genetics! The complex phenotype of CASPR2 deficiency disorder: https://…

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