Matches in Nanopublications for { ?s ?p "[We report a novel G61R SOD1 mutation in a patient with a distinct phenotype including prominent lower motor neuron dysfunction, proximal weakness and atrophy with asymmetrical onset in the thigh and buttock and relentless clinical course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_assertion description "[We report a novel G61R SOD1 mutation in a patient with a distinct phenotype including prominent lower motor neuron dysfunction, proximal weakness and atrophy with asymmetrical onset in the thigh and buttock and relentless clinical course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_provenance.
- NP440724.RAfCYYX_Po-PmvKxooYv-HUyiMZSfZ3D46LQa5qlQkcoE130_assertion description "[We report a novel G61R SOD1 mutation in a patient with a distinct phenotype including prominent lower motor neuron dysfunction, proximal weakness and atrophy with asymmetrical onset in the thigh and buttock and relentless clinical course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440724.RAfCYYX_Po-PmvKxooYv-HUyiMZSfZ3D46LQa5qlQkcoE130_provenance.
- NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_assertion description "[We report a novel G61R SOD1 mutation in a patient with a distinct phenotype including prominent lower motor neuron dysfunction, proximal weakness and atrophy with asymmetrical onset in the thigh and buttock and relentless clinical course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.