Gene table: search width pubmed_id = 26870663


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Myasthenic syndrome, congenital, 23, presynaptic - (AR)
11.31
26870663
SLC25A1 (22q11.21)
Solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1(M)
* Presynaptic congenital myasthenic syndrome 23 - CMS23