Matches in Nanopublications for { ?s ?p "[A protein truncating mutation was identified in the gene CC2D1A in nine consanguineous families with severe autosomal recessive mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- NP126775.RAAFUHZKVjzvEVqsWEtulGEAfnfEQA5ekIsSy-NxAOq5I130_assertion description "[A protein truncating mutation was identified in the gene CC2D1A in nine consanguineous families with severe autosomal recessive mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126775.RAAFUHZKVjzvEVqsWEtulGEAfnfEQA5ekIsSy-NxAOq5I130_provenance.
- assertion description "[A protein truncating mutation was identified in the gene CC2D1A in nine consanguineous families with severe autosomal recessive mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP189956.RAgFYNZuPMK_N1h1QN3aUNjep37y9R3O_vviw1NkVUez8130_assertion description "[A protein truncating mutation was identified in the gene CC2D1A in nine consanguineous families with severe autosomal recessive mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189956.RAgFYNZuPMK_N1h1QN3aUNjep37y9R3O_vviw1NkVUez8130_provenance.
- NP212046.RAfHOQlkZPlBLA3AtY0N_8iWXeSJraPGcVjajLiFM58Jo130_assertion description "[A protein truncating mutation was identified in the gene CC2D1A in nine consanguineous families with severe autosomal recessive mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212046.RAfHOQlkZPlBLA3AtY0N_8iWXeSJraPGcVjajLiFM58Jo130_provenance.