Investigation of NOTCH rare SNV as protective modifiers in Duchenne muscular dystr...
High throughput genomic edition to investigate neurodevelopmental disorders ass...
Identifying sickle cell anemia modifying genes by exome analysis
Congenital adrenal hyperplasia: new mutations and their effects on the enzymatic a...
Investigation of the etiological relevance of novel candidate genes to orofacial c...
Studies on Amyotrophic Lateral Sclerosis type 8 physiopathology through induced pl...