Our new case report of TRIM32-related LGMDR8 is now available on @FrontNeurol , with a literature review of LGMDR8 clinical & instrumental data associated to the so far known TRIM32 variants 🧬 @CentDinoFerrari @LaStatale @policlinicoMI @TwittAuxologic
Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy: Limb-girdle muscular dystrophy autosomal recessive 8 (LGMDR8) is a rare clinical manifestation caused by the presence of biallelic variants in… https://t.co/w5hgL0uXKO…
New Research: Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy: Limb-girdle muscular dystrophy autosomal recessive 8 (LGMDR8) is a rare clinical manifestation caused by the presence of biallelic variants in… https://t.c