The congenital melanocytic nevus (CMN) is a generally sporadic malformation of the skin, due to mutations that take place during pregnancy. The mutant cells spread and proliferate be...
€ 36030 PledgedLarge congenital melanocytic nevusSupport!funding € 30milestone goal 7.000
€ 1141 PledgedSteinert myotonic dystrophySupport!Research project: How a better characterization of the genotype-phenotype relation will help in applying early symptomatic treatments for Steinert Myotonic Dystrophy patients OVER...funding € 1.141milestone goal 8.800
A. RenieriWHAT IS FOXG1? FOXG1 is a rare genetic mutation of the FOXG1 gene that impacts brain development and function. This severe neurological condition is characterized by seizures, inabi...funding € 7.501milestone goal 154k