Matches in Nanopublications for { ?s ?p "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP294780.RAR2R_m5rc1WEXr2RK-kj2I0YKQbub1ZWUJQZe2sRlYR4130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294780.RAR2R_m5rc1WEXr2RK-kj2I0YKQbub1ZWUJQZe2sRlYR4130_provenance.
- NP294781.RAm70ffbq6bLTGTx8MW9o2QmN_5ypyJN3Q-9M6kRIl7E8130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294781.RAm70ffbq6bLTGTx8MW9o2QmN_5ypyJN3Q-9M6kRIl7E8130_provenance.
- NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.
- NP294779.RAzTMrI9UWIt8qGbCmzMlebOXKMWBvugLhAV2aJFKrwNo130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294779.RAzTMrI9UWIt8qGbCmzMlebOXKMWBvugLhAV2aJFKrwNo130_provenance.