Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Oscar Jackson"'
Autor:
Jonathan Gilley, Oscar Jackson, Menelaos Pipis, Mehrdad A Estiar, Ammar Al-Chalabi, Matt C Danzi, Kristel R van Eijk, Stephen A Goutman, Matthew B Harms, Henry Houlden, Alfredo Iacoangeli, Julia Kaye, Leandro Lima, Queen Square Genomics, John Ravits, Guy A Rouleau, Rebecca Schüle, Jishu Xu, Stephan Züchner, Johnathan Cooper-Knock, Ziv Gan-Or, Mary M Reilly, Michael P Coleman
Publikováno v:
eLife, Vol 10 (2021)
SARM1, a protein with critical NADase activity, is a central executioner in a conserved programme of axon degeneration. We report seven rare missense or in-frame microdeletion human SARM1 variant alleles in patients with amyotrophic lateral sclerosis
Externí odkaz:
https://doaj.org/article/983da56b2cb8455c8e30f44db1e45752
Autor:
Leandro Lima, Stephen A. Goutman, Oscar Jackson, Henry Houlden, Menelaos Pipis, Mehrdad Asghari Estiar, Ziv Gan-Or, Kristel R. van Eijk, Rebecca Schüle, Ammar Al-Chalabi, Julia Kaye, Mary M. Reilly, Matthew B. Harms, Stephan Züchner, John Ravits, Jishu Xu, Johnathan Cooper-Knock, Queen Square Genomics, Jonathan Gilley, Matt C. Danzi, Alfredo Iacoangeli, Michael P. Coleman, Guy A. Rouleau
Publikováno v:
eLife, Vol 10 (2021)
eLife 10, e70905 (2021). doi:10.7554/eLife.70905
eLife
eLife 10, e70905 (2021). doi:10.7554/eLife.70905
eLife
SARM1, a protein with critical NADase activity, is a central executioner in a conserved programme of axon degeneration. We report seven rare missense or in-frame microdeletion human SARM1 variant alleles in patients with amyotrophic lateral sclerosis
Autor:
Stephen A. Goutman, Leandro Lima, Menelaos Pipis, Matthew B. Harms, Julia Kaye, Johnathan Cooper-Knock, Queen Square Genomics, Ziv Gan-Or, Kristel R. van Eijk, Oscar Jackson, Matt C. Danzi, Jishu Xu, Rebecca Schüle, Ammar Al-Chalabi, Mehrdad Asghari Estiar, Henry Houlden, Jonathan Gilley, Stephan Züchner, Mary M. Reilly, Alfredo Iacoangeli, Michael P. Coleman, John Ravits, Guy A. Rouleau
SARM1, a protein with critical NADase activity, is a central executioner in a conserved programme of axon degeneration. We report seven rare missense or in-frame microdeletion human SARM1 variant alleles in patients with amyotrophic lateral sclerosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::351ef341eefec0bd7e8e35362dc95522
https://doi.org/10.1101/2021.06.17.21258268
https://doi.org/10.1101/2021.06.17.21258268