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Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia

✍ Scribed by Ljubica Caldovic; Hiroki Morizono; Maria Gracia Panglao; Sabrina F. Cheng; Seymour Packman; Mendel Tuchman

Publisher
Springer
Year
2003
Tongue
English
Weight
298 KB
Volume
112
Category
Article
ISSN
0340-6717

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## Summary The aim of this study was to identify possible disease‐associated mutations in the canine homologue of the polycystic kidney disease gene 1 (__PKD1__) in Bull Terriers with autosomal dominant polycystic kidney disease. Messenger RNA was obtained from the blood or renal tissue of five Bul