A Novel Missense Mutation in Codon 218 of the Albumin Gene...

Journal of Clinical Endocrinology & Metabolism 1997 / 10 Vol. 82; Iss. 10

A Novel Missense Mutation in Codon 218 of the Albumin Gene in a Distinct Phenotype of Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Kindred

Wada, Norio, Chiba, Hitoshi, Shimizu, Chikara, Kijima, Hiromichi, Kubo, Mitsumasa, Koike, Takao
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Volume:
82
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jcem.82.10.4276
Date:
October, 1997
File:
PDF, 2.81 MB
1997
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