Title : A point mutation in the albumin gene in a Chinese patient with familial dysalbuminemic hyperthyroxinemia.

Pub. Date : 1999 Oct

PMID : 10526251






1 Functional Relationships(s)
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Protein Name
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1 Direct sequencing of the albumin gene showed a guanine to adenosine transition in the second nucleotide of codon 218, resulting in a substitution of histidine (CAC) for the normal arginine (CGC) in one of the two alleles in the patient. Histidine albumin Homo sapiens