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Rare Neurodegenerative Diseases

European Society of Human Genetics. Glasgow, 6-9 June 2015

Carmen Espinós and Eduardo Calpena have attended to the conference of the European Society of Human Genetics held in Glasgow in June 6th-9th. They presented a written communication related to the research about Neurodegeneration Brain Iron Accumulation (NBIA) disorders and an oral presentation about the role of junctophilin-1 as genetic modifier of the GDAP1 gene. Eduardo Calpena was chosen as candidate for young investigator awards. 

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