Filamin C The FLNC gene codify for the muscle-specific filamin isoform. It is involved in a form of autosomal dominant myofibrillar myopathy (MFM) described by Vorgerd et al. in 2005 (27). Patients presented with slow progressive skeletal-muscle weakness, beginning in the lower extremities, which is compatible with the clinical signs of LGMD. ZASP Z-band alternatively spliced PDZ-motif containing protein is a sarcomeric protein expressed in human cardiac

and skeletal muscle at the Z-disk (28). Several mutations in ZASP gene have been Inhibitors,research,lifescience,medical identified as responsible for different dominant disorders: MFM and dilated cardiomyopathy (29–31). The clinical phenotype in patients is heterogeneous, with variable age of onset, proximal or distal presentation and variable occurrence of cardiomyopathy. Inhibitors,research,lifescience,medical Kinectin 1 It is a 160kDa transmembrane protein located on the cytoplasmic vesicles of the endoplasmic reticulum. This is probably present on the vesicles that operate the transport of proteins from the endoplasmic

Inhibitors,research,lifescience,medical Protease Inhibitor Library concentration reticulum to the Golgi. It may mediate the binding between kinesin and vesicle membrane to be transported (32). To date no disease has been linked to mutation in kinectin 1 gene. Enolase 3-b The enolase enzyme catalyze the conversion of 2-phosphoglycerate into 2-phosphoenolpyruvate, and the beta isoform is muscle specific. In 2001, Comi et al. (33) described a patient with a metabolic myopathy showing myalgia, fatigue Inhibitors,research,lifescience,medical and stress-induced weakness. This patient resulted compound heterozygous for two missense mutations in ENO3 gene. TRIM11 and TRIM17 These are two small cytosolic proteins belonging to tripartite motif containing protein family (TRIM) as the muscular dystrophy 2H gene TRIM32. The two genes map at

Inhibitors,research,lifescience,medical chromosome 1 in the critical region for the congenital muscular dystrophy 1B (MDC1B, OMIM #604801). The disease is characterized by proximal muscle weakness with hypertrophy, respiratory failure and increased CK serum levels. ζ-sarcoglycan It is a well known gene whose protein product belongs to sarcoglycans protein family (34). It has been demonstrated its ability to form an alternative complex with α, β and δ in different tissues if γ-sarcoglycan Cell press is absent. Four sarcoglycans gene are mutated in LGMDs (α, β, γ and δ) and ε- is the gene mutated in the myoclonic dystonic syndrome (DYT11, 35). OZZ It is a small muscle specific protein and is a member of SOCS proteins family. In 2004, Nastasi et al. demonstrated the involvement of OZZ in an active E3-ligase complex in which β-catenin serves as substrate in vivo. OZZ knock-out mice show a muscle phenotype with an increased nuclei centralization and misalignment of myofibrils (36). Mutation scanning We analyzed all coding exons and flanking introns and verified whether each variation was present in DB-SNP (NCBI) or not.