Matches in Nanopublications for { ?s ?p "[Mutations of the myelin protein zero (MPZ) gene have been associated with CMT1B, Dejerine-Sottas disease, and congenital hypomyelination, which are inherited demyelinating neuropathies characterized by different clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion description "[Mutations of the myelin protein zero (MPZ) gene have been associated with CMT1B, Dejerine-Sottas disease, and congenital hypomyelination, which are inherited demyelinating neuropathies characterized by different clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- assertion description "[Mutations of the myelin protein zero (MPZ) gene have been associated with CMT1B, Dejerine-Sottas disease, and congenital hypomyelination, which are inherited demyelinating neuropathies characterized by different clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion description "[Mutations of the myelin protein zero (MPZ) gene have been associated with CMT1B, Dejerine-Sottas disease, and congenital hypomyelination, which are inherited demyelinating neuropathies characterized by different clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.