stahp - betting world cup
$800.00
All patients were homozygous for the c. ngamentogel 2 335dupG (p. cara bisa split dalam satu hari Cys112Trpfs*11) mutation in the SOD1 gene with completely decreased enzyme activity This case series is the biggest data collection of the new recent clinical entity described as Spastic Tetraplegia and Axial Hypotonia (STAHP) due to SOD1 deficiency