QuickView for SYT2;jsessionid=704E9D2BF58C58DDE54B4A67F9D6DD90 (gene)

1. Exome sequencing and microarray identified a novel large exonic deletion in SYT2 gene in an ultra-ra…
2. Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations.
3. Identification of a Novel de Novo Variant in the SYT2 Gene Causing a Rare Type of Distal Hereditary …
4. Biallelic loss of function variants in SYT2 cause a treatable congenital onset presynaptic myastheni…
5. Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly c…

There were no clinical trials for SYT2;jsessionid=704E9D2BF58C58DDE54B4A67F9D6DD90