Hypermutability of CpG dinucleotides in the propeptide-encoding sequence of the human albumin gene.

An electrophoretically slow albumin variant was detected with a phenotype frequency of about 1:1000 in Sweden and was also found in a family of Scottish descent from Kaikoura, New Zealand, and in five families in Tradate, Italy. Structural study established that the major variant component was argin...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Brennan, S O, Arai, K, Madison, J, Laurell, C B, Galliano, M, Watkins, S, Peach, R, Myles, T, George, P, Putnam, F W
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1990
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC54013/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2339130/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.10.3909
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