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RT @DiseaseGenes: RT @JamesFasham: De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neur…
RT @DiseaseGenes: RT @JamesFasham: De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neur…
Mutacions en el gen RNU4-2, codifica l'ARN nuclear petit U4, un component crític de l'espliceosoma, relacionades amb discapacitat intel·lectual. https://t.co/xx2YxOcJ1C
RT @NatureMedicine: Mutations in a small noncoding gene called #RNU4-2 are responsible for one of the most common of the #neurodevelopmenta…