Matches in Nanopublications for { ?s ?p "[We have identified by sequence analysis a novel missense heterozygous mutation in the NKX2-5 gene, specifically a substitution of glutamine for proline at codon 160, in a Moroccan family, the affected members having a deficiency of the floor of the oval fossa and atrioventricular block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP682503.RArK4DZ0D3_DlY46x_DjOOubCRYCIAKeKEJi5Wavt4dfU130_assertion description "[We have identified by sequence analysis a novel missense heterozygous mutation in the NKX2-5 gene, specifically a substitution of glutamine for proline at codon 160, in a Moroccan family, the affected members having a deficiency of the floor of the oval fossa and atrioventricular block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682503.RArK4DZ0D3_DlY46x_DjOOubCRYCIAKeKEJi5Wavt4dfU130_provenance.
- NP333978.RAbooGgZrq5d2CZKM3mYp0qlZx1LKxuYsK3qExvfNY16E130_assertion description "[We have identified by sequence analysis a novel missense heterozygous mutation in the NKX2-5 gene, specifically a substitution of glutamine for proline at codon 160, in a Moroccan family, the affected members having a deficiency of the floor of the oval fossa and atrioventricular block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333978.RAbooGgZrq5d2CZKM3mYp0qlZx1LKxuYsK3qExvfNY16E130_provenance.
- NP585584.RAv0a66M1jNi6x3AdGt1mS-DGS0jpT1So2OlcDJBMKS88130_assertion description "[We have identified by sequence analysis a novel missense heterozygous mutation in the NKX2-5 gene, specifically a substitution of glutamine for proline at codon 160, in a Moroccan family, the affected members having a deficiency of the floor of the oval fossa and atrioventricular block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585584.RAv0a66M1jNi6x3AdGt1mS-DGS0jpT1So2OlcDJBMKS88130_provenance.