Matches in Nanopublications for { ?s ?p "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP357020.RATPcslX2pK-xjthmJw9WZS6UG0Sl-z8OjKf275997LV0130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357020.RATPcslX2pK-xjthmJw9WZS6UG0Sl-z8OjKf275997LV0130_provenance.
- NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.
- NP821842.RAy5UHX9cpcy58jncsHL_xdlJuGsEs7q-pSUXw8zt6OKI130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821842.RAy5UHX9cpcy58jncsHL_xdlJuGsEs7q-pSUXw8zt6OKI130_provenance.
- NP827188.RAGzCnFBuJFRL78aNHkOAjqwaFdwyzFY0ZZgG-AE08DAw130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827188.RAGzCnFBuJFRL78aNHkOAjqwaFdwyzFY0ZZgG-AE08DAw130_provenance.
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- NP1071537.RAsptu4IEyyJ-FpAIZVOY2cj765m-mUf9KZhtlIXTc8eA130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1071537.RAsptu4IEyyJ-FpAIZVOY2cj765m-mUf9KZhtlIXTc8eA130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.