Matches in Nanopublications for { ?s ?p "[Based on previous reports the frequency of co-segregating recessive chloride channel (CLCN1) mutations in families with myotonic dystrophy type 2 (DM2) was suspected to be increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_assertion description "[Based on previous reports the frequency of co-segregating recessive chloride channel (CLCN1) mutations in families with myotonic dystrophy type 2 (DM2) was suspected to be increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_provenance.
- NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_assertion description "[Based on previous reports the frequency of co-segregating recessive chloride channel (CLCN1) mutations in families with myotonic dystrophy type 2 (DM2) was suspected to be increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.