Date: 2016 / Author/Creator: Fowler, Brian - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Date 2016 Author/Creator Fowler, Brian

1. Functional characterization of missense mutations in severe methylenetetrahydrofolate reductase deficiency using a human expression system. Issue 2 (14th October 2016)

Authors:: Burda, Patricie; Suormala, Terttu; Heuberger, Dorothea; Schäfer, Alexandra; Fowler, Brian; Froese, D. Sean; Baumgartner, Matthias R.
Journal:: Journal of inherited metabolic disease
Issue:: Volume 40:Issue 2(2017)
Page Start:: 297
Record Type:: Journal Article
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2. Molecular Genetic Characterization of 151 Mut‐Type Methylmalonic Aciduria Patients and Identification of 41 Novel Mutations in MUT. Issue 8 (23rd May 2016)

Authors:: Forny, Patrick; Schnellmann, Anne‐Sophie; Buerer, Celine; Lutz, Seraina; Fowler, Brian; Froese, D. Sean; Baumgartner, Matthias R.
Journal:: Human mutation
Issue:: Volume 37:Issue 8(2016)
Page Start:: 745
Record Type:: Journal Article
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3. Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency. Issue 5 (18th March 2016)

Authors:: Froese, D. Sean; Huemer, Martina; Suormala, Terttu; Burda, Patricie; Coelho, David; Guéant, Jean‐Louis; Landolt, Markus A.; Kožich, Viktor; Fowler, Brian; Baumgartner, Matthias R.
Journal:: Human mutation
Issue:: Volume 37:Issue 5(2016)
Page Start:: 427
Record Type:: Journal Article
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