Matches in Nanopublications for { ?s ?p "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.
- assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_provenance.
- NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_provenance.
- NP6551.RAu0tA83cIu3JgVJr1uZbKzM3ydAtu7vbUd-ZoJExhBOo130_assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6551.RAu0tA83cIu3JgVJr1uZbKzM3ydAtu7vbUd-ZoJExhBOo130_provenance.
- NP1381910.RACMIdn0ZdcsML-CbzdN08HpNNveFFbcROvKOAYAe_WJ8130_assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1381910.RACMIdn0ZdcsML-CbzdN08HpNNveFFbcROvKOAYAe_WJ8130_provenance.
- NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.