Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus
Michael F. Hammer, Yanling Pan, Medhane Cumbay, Manuela Pendziwiat, Zaid Afawi, Hadassah Goldberg-Stern, Laurel Johnstone, Ingo Helbig, Theodore R. Cummins
Research output: Contribution to journal › Article › peer-review
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