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pro vyhledávání: '"Jill C Skrabal"'
Publikováno v:
SAGE Open Medical Case Reports, Vol 2 (2014)
Introduction: Ornithine transcarbamylase deficiency is the most common inherited disorder of the urea cycle, has a variable phenotype, and is caused by mutations in the OTC gene. We report three cases of ornithine transcarbamylase deficiency to illus
Externí odkaz:
https://doaj.org/article/2d5c657000b143cc8c4d9db858c55ca5