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