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Inborn errors of metabolism with a focus on functional analysis of a special mutation in MCCB causing 3-Methylcrotonyl-CoA carboxylase deficiency, and MMADHC in intracellular vitamin B12 metabolism, a gene in which mutations can lead to three Different phenotypes - Zurich Open Repository and Archive


Stucki, M. Inborn errors of metabolism with a focus on functional analysis of a special mutation in MCCB causing 3-Methylcrotonyl-CoA carboxylase deficiency, and MMADHC in intracellular vitamin B12 metabolism, a gene in which mutations can lead to three Different phenotypes. 2010, University of Zurich, Faculty of Science.

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Item Type:Dissertation
Referees:Verrey F, Baumgartner M R, Hennet T, Fowler B
Communities & Collections:04 Faculty of Medicine > Center for Integrative Human Physiology
04 Faculty of Medicine > University Children's Hospital Zurich > Medical Clinic
Dewey Decimal Classification:570 Life sciences; biology
610 Medicine & health
Language:English
Date:2010
Deposited On:16 Jul 2010 08:38
Last Modified:05 Apr 2016 14:11
Additional Information:Inborn errors of metabolism with a focus on functional analysis of a special mutation in MCCB causing 3-Methylcrotonyl-CoA carboxylase deficiency, and MMADHC in intracellular vitamin B₁₂ metabolism, a gene in which mutations can lead to three different phenotypes / von Martin Stucki. - Zürich, 2010.
Related URLs:http://opac.nebis.ch/F/?local_base=NEBIS&con_lng=GER&func=find-b&find_code=SYS&request=006160359

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