Open AccessA Novel Missense Mutation in Codon 218 of the Albumin Gene in a Distinct Phenotype of Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Kindred
Author(s) -
N. Wada
Publication year - 1997
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.82.10.3246
Subject(s) - missense mutation , cytosine , proband , albumin , guanine , medicine , transition (genetics) , genetics , amino acid , endocrinology , microbiology and biotechnology , gene , mutation , biology , nucleotide
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