Hamanaka et al., 2020 - De Novo Truncating Variants in the Last Exon of SEMA6B Cause Progressive Myoclonic Epilepsy. American journal of human genetics   106(4):549-558 Full text @ Am. J. Hum. Genet.
2 Genes / Markers
Marker Type Symbol Name
Gene sema6ba sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6Ba
Gene sema6bb sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6Bb
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