A mouse model with a frameshift mutation in the nuclear factor i/x (nfix) gene has phenotypic features of marshall‐smith syndrome

HIGHLIGHTS

• who: Kreepa G. Kooblall et al. from the Academic Endocrine Unit, Radcliffe Department of Medicine, Oxford Centre for Diabetes, Endocrinology and Metabolism (OCDEM), University of Oxford, Oxford, UK have published the Article: A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshallu2010Smith Syndrome, in the Journal: (JOURNAL)
• what: The authors report three Nfix mouse models with three different targeted mutations in exon 7 of the Nfix gene, which are representative of the most frequent NFIX mutations observed in MSS patients.

SUMMARY

 



If you want to have access to all the content you need to log in!

Thanks :)

Username or Email

Password

Remember me

Lost your password?

If you don't have an account, you can create one here.