Matches in Nanopublications for { ?s ?p "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_provenance.
- NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.
- assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_provenance.
- assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.