Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Megan M. Krogman"'
Autor:
Megan M. Krogman, Christian L. Lorson, Michael L. Garcia, Ferrill F. Rose, Hansjörg Rindt, Spencer M. Vale, Desire M. Buckley
Publikováno v:
Neuromuscular Disorders. 22:277-285
Spinal Muscular Atrophy (SMA) is a devastating neurodegenerative disease and is a leading genetic cause of infantile death. SMA is caused by the homozygous loss of Survival Motor Neuron-1 (SMN1). The presence of a nearly identical copy gene called SM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cd437dedc670b62ac61fe4ca1039cf1
https://doi.org/10.1016/j.nmd.2011.10.012
https://doi.org/10.1016/j.nmd.2011.10.012
Publikováno v:
Biochemical and biophysical research communications. 417(1)
Spinal Muscular Atrophy (SMA), an autosomal recessive neuromuscular disorder, is the leading genetic cause of infant mortality. SMA is caused by the homozygous loss of Survival Motor Neuron-1 (SMN1). SMA, however, is not due to complete absence of SM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cbd5b31c9979f85593dfce951f023bb
https://pubmed.ncbi.nlm.nih.gov/22172949
https://pubmed.ncbi.nlm.nih.gov/22172949
Autor:
Christian L. Lorson, Megan M. Krogman, Mary J. Wetz, Erkan Y. Osman, Jacqueline J. Glascock, Monir Shababi
Spinal muscular atrophy (SMA), an autosomal recessive neuromuscular disorder, is the leading genetic cause of infant mortality. SMA is caused by the homozygous loss of Survival Motor Neuron-1 (SMN1). In humans, a nearly identical copy gene is present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64e8ad53627f8a1da4049f1979953579
https://europepmc.org/articles/PMC3300100/
https://europepmc.org/articles/PMC3300100/
Autor:
Rindt H; Department of Veterinary Pathobiology, University of Missouri, Columbia, MO 65211, USA., Buckley DM, Vale SM, Krogman M, Rose FF Jr, Garcia ML, Lorson CL
Publikováno v:
Neuromuscular disorders : NMD [Neuromuscul Disord] 2012 Mar; Vol. 22 (3), pp. 277-85. Date of Electronic Publication: 2011 Nov 10.