Matches in Nanopublications for { ?s ?p "[In this study we analyzed the genotype and phenotype of individuals from two unrelated families with HCM in which the affected individuals have the same missense mutation in exon 13 (G1208A) of the coding sequence for beta MHC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP653316.RAembhsml0L17g0Rs5mS5zaleOzKfQq4s7hYznBzDJlTI130_assertion description "[In this study we analyzed the genotype and phenotype of individuals from two unrelated families with HCM in which the affected individuals have the same missense mutation in exon 13 (G1208A) of the coding sequence for beta MHC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP653316.RAembhsml0L17g0Rs5mS5zaleOzKfQq4s7hYznBzDJlTI130_provenance.
- NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_assertion description "[In this study we analyzed the genotype and phenotype of individuals from two unrelated families with HCM in which the affected individuals have the same missense mutation in exon 13 (G1208A) of the coding sequence for beta MHC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_provenance.
- NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_assertion description "[In this study we analyzed the genotype and phenotype of individuals from two unrelated families with HCM in which the affected individuals have the same missense mutation in exon 13 (G1208A) of the coding sequence for beta MHC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_provenance.