Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees

Por Zlatic, Stephanie A., Vrailas-Mortimer, Alysia, Gokhale, Avanti, Carey, Lucas J., Scott, Elizabeth, Burch, Reid, McCall, Morgan M., Rudin-Rush, Samantha, Davis, John Bowen, Hartwig, Cortnie, Werner, Erica, Li, Lian, Petris, Michael, Faundez, Victor
Publicado no Cell Syst (2018)

The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors

Por Comstra, Heather S, McArthy, Jacob, Rudin-Rush, Samantha, Hartwig, Cortnie, Gokhale, Avanti, Zlatic, Stephanie A, Blackburn, Jessica B, Werner, Erica, Petris, Michael, D’Souza, Priya, Panuwet, Parinya, Barr, Dana Boyd, Lupashin, Vladimir, Vrailas-Mortimer, Alysia, Faundez, Victor
Publicado no eLife (2017)