Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Christie Sapp Savas"'
Autor:
Blaine R. Roberts, Roman S. Polishchuk, Vladimir Lupashin, Victor Faundez, Daniel N. Cox, Alysia D. Vrailas-Mortimer, Gretchen Macias Mendez, Stephanie A. Zlatic, Cortnie Hartwig, Avanti Gokhale, Mafalda Concilli, Laura Palmer, Nicole Shearing, Jacob McArthy, Savanah Taylor, Lindsey Margewich, Samantha Rudin-Rush, Ramon A. Jorquera, Christie Sapp Savas, Shatabdi Bhattacharjee, Amanda A. H. Freeman, Erica Werner
Publikováno v:
J Neurosci
Rare genetic diseases preponderantly affect the nervous system causing neurodegeneration to neurodevelopmental disorders. This is the case for both Menkes and Wilson disease, arising from mutations in ATP7A and ATP7B, respectively. The ATP7A and ATP7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::383c44d1ac297837410e83e4223bfea3
https://doi.org/10.1523/jneurosci.1284-20.2020
https://doi.org/10.1523/jneurosci.1284-20.2020
Autor:
Roman R Polishchuk, Lindsey Margewich, Blaine R. Roberts, Samantha Rudin-Rush, Vladimir Lupashin, Cortnie Hartwig, Stephanie A. Zlatic, Daniel N. Cox, Gretchen Macias Mendez, Christie Sapp Savas, Ramon A. Jorquera, Victor Faundez, Alysia D. Vrailas-Mortimer, Laura Palmer, Avanti Gokhale, Mafalda Concilli, Jacob McArthy, Nicole Shearing, Shatabdi Bhattacharjee, Amanda A. H. Freeman, Savanah Taylor
Rare genetic diseases preponderantly affect the nervous system with phenotypes spanning from neurodegeneration to neurodevelopmental disorders. This is the case for both Menkes and Wilson disease, arising from mutations in ATP7A and ATP7B, respective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f49910bc38f32f43f814ea47192cc4c
https://doi.org/10.1101/2020.05.22.110627
https://doi.org/10.1101/2020.05.22.110627
