Matches in Nanopublications for { ?s ?p "[This autosomal dominant inherited disorder is caused by mutations in the gene LEMD3 on chromosome 12q14, which induces a rather heterogeneous clinical phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 1 of
1
with 100 items per page.
- NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_assertion description "[This autosomal dominant inherited disorder is caused by mutations in the gene LEMD3 on chromosome 12q14, which induces a rather heterogeneous clinical phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_provenance.