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RARE REVOLUTION

This entry was posted on 13th December 2016 by Jenna

The function of most of our 20,000 genes is currently unknown, and we know even less about what happens if each gene has a mutation. In ‘clinical spotlight’ feature for the Winter edition of Rare Revolution Magazine , the DMDD and IMPC consortia talk about the role mouse embryo phenotyping plays in understanding the genetic basis of rare disease, and the efforts to make their data freely available to all.

Read the full Rare Revolution article or subscribe to the magazine for free to receive future issues by email.

 

The Rare Revolution Winter 2016 edition.

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This entry was posted on 13th December 2016 by Jenna

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