Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Nathaniel E. Goldman"'
Autor:
Vandana A Gupta, Karim Hnia, Laura L Smith, Stacey R Gundry, Jessica E McIntire, Junko Shimazu, Jessica R Bass, Ethan A Talbot, Leonela Amoasii, Nathaniel E Goldman, Jocelyn Laporte, Alan H Beggs
Publikováno v:
PLoS Genetics, Vol 9, Iss 6, p e1003583 (2013)
X-linked myotubular myopathy (XLMTM) is a congenital disorder caused by mutations of the myotubularin gene, MTM1. Myotubularin belongs to a large family of conserved lipid phosphatases that include both catalytically active and inactive myotubularin-
Externí odkaz:
https://doaj.org/article/86d1bea72b0448b58d06332a5ecc317c
Autor:
Karim Hnia, Jessica E. McIntire, Leonela Amoasii, Laura L. Smith, Ethan A. Talbot, Junko Shimazu, Vandana Gupta, Jocelyn Laporte, Jessica R. Bass, Alan H. Beggs, Nathaniel E. Goldman, Stacey R. Gundry
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 9, Iss 6, p e1003583 (2013)
PLoS Genetics, Vol 9, Iss 6, p e1003583 (2013)
X-linked myotubular myopathy (XLMTM) is a congenital disorder caused by mutations of the myotubularin gene, MTM1. Myotubularin belongs to a large family of conserved lipid phosphatases that include both catalytically active and inactive myotubularin-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2e48f92ceead01e1839b39408f80dfc
https://pubmed.ncbi.nlm.nih.gov/23818870
https://pubmed.ncbi.nlm.nih.gov/23818870