Matches in Nanopublications for { ?s ?p "[Dejerine-Sottas disease, also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene of the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Dejerine-Sottas disease, also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene of the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Dejerine-Sottas disease, also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene of the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Dejerine-Sottas disease, also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene of the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_assertion description "[Dejerine-Sottas disease, also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene of the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_provenance.
- NP1323784.RAskRMeuPpQQhHuOz9Ah2Ooiu-Ia2ohkcHO10R7Gs-4ck130_assertion description "[Dejerine-Sottas disease, also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene of the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323784.RAskRMeuPpQQhHuOz9Ah2Ooiu-Ia2ohkcHO10R7Gs-4ck130_provenance.
- NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_assertion description "[Dejerine-Sottas disease, also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene of the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.