Molecular genetic study of human arginase deficiency

We have explored the molecular pathology in 28 individuals homozygous or heterozygous for liver arginase deficiency (hyperargininemia) by a combination of Southern analysis, western blotting, DNA sequencing, and PCR. This cohort represents the majority of arginase-deficient individuals worldwide. On...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Grody, Wayne W., Klein, Deborah, Dodson, Amy E., Kern, Rita M., Wissmann, Paul B., Goodman, Barbara K., Bassand, Patrick, Marescau, Bert, Kang, Soo-Sang, Leonard, James V., Cederbaum, Stephen D.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1992
Gaiak:
Original Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682550/
https://ncbi.nlm.nih.gov/pubmed/1598908
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