Family studies in ornithine transcarbamylase deficiency.

Six families with at least one infant each with confirmed ornithine transcarbamylase deficiency were investigated by DNA analysis. All the affected sons had died, and no DNA had been stored. Using the restriction endonucleases MspI and Bam HI three restriction fragment length polymorphisms were dete...

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Hlavní autoři: Svirklys, L G, Wilcken, B, Hammond, J, Mackinlay, A G, O'Sullivan, W J
Médium: Artigo
Jazyk:Inglês
Vydáno: 1988
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1778759/
https://ncbi.nlm.nih.gov/pubmed/3355210
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