Matches in Nanopublications for { ?s ?p "[Mutations in the SH3TC2 gene are a frequent cause of demyelinating hereditary neuropathy among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_assertion description "[Mutations in the SH3TC2 gene are a frequent cause of demyelinating hereditary neuropathy among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.
- assertion description "[Mutations in the SH3TC2 gene are a frequent cause of demyelinating hereditary neuropathy among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_assertion description "[Mutations in the SH3TC2 gene are a frequent cause of demyelinating hereditary neuropathy among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_provenance.
- NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_assertion description "[Mutations in the SH3TC2 gene are a frequent cause of demyelinating hereditary neuropathy among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.