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Publication | Open Access

Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID

DOIFull Paper Access

41

Citations

9

References

2017

Year

Silke Redler, Tim M. Strom, Thomas Wieland, Kirsten Cremer, Hartmut Engels, Felix Distelmaier, Jörg Schaper, Alma Küchler, Johannes R. Lemke, Stephanie Jeschke,
European Journal of Human Genetics

References

YearCitations

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