Literature DB >> 1861449

Ornithine transcarbamylase deficiency: findings and treatment in a symptomatic female heterozygote.

C Soulpis1, D Markosoglou, F Papadelis, A Caraboula, S Giouroukos, A Skarpalezou, S Missìou-Tsagarakis, H Michelakakis.   

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Year:  1991        PMID: 1861449     DOI: 10.1007/bf01804398

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


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  2 in total

Review 1.  Treatment of urea cycle disorders.

Authors:  M L Batshaw; P S Monahan
Journal:  Enzyme       Date:  1987

2.  Natural history of symptomatic partial ornithine transcarbamylase deficiency.

Authors:  P C Rowe; S L Newman; S W Brusilow
Journal:  N Engl J Med       Date:  1986-02-27       Impact factor: 91.245

  2 in total

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