Hereditäre SPAST (SPG4)ische Paraplegie (HSP) oder SPAST (SPG4)ische Spinalparalyse (SPG) – autosomal dominant

Basis-Diagnostik

ATL1 (SPG3a), BSCL2 (SPG17), HSPD1 (SPG13), KIF5A (SPG10), NIPA1 (SPG6), REEP1 (SPG31), RTN2 (SPG12), SLC33A1 (SPG42), SPAST (SPG4), ZFYVE27 (SPG33)

Menü