Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

M Huemer, R Mulder-Bleile, P Burda… - Journal of inherited …, 2016 - Springer
Background Severe methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare
inborn defect disturbing the remethylation of homocysteine to methionine (< 200 reported …
被引用次数：68 相关文章

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

M Huemer, R Mulder-Bleile, P Burda… - J. Inherit. Metab …, 2016 - kups.ub.uni-koeln.de
Background Severe methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare
inborn defect disturbing the remethylation of homocysteine to methionine (< 200 reported …

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency.

M Huemer, R Mulder-Bleile, P Burda… - Journal of inherited …, 2016 - avesis.istanbul.edu.tr
Background Severe methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare
inborn defect disturbing the remethylation of homocysteine to methionine (< 200 reported …

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency.

M Huemer, R Mulder-Bleile, P Burda… - Journal of Inherited …, 2015 - europepmc.org
Background Severe methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare
inborn defect disturbing the remethylation of homocysteine to methionine (< 200 reported …

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

M Huemer, R Mulder-Bleile, P Burda… - Journal of inherited …, 2016 - pubmed.ncbi.nlm.nih.gov
Background Severe methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare
inborn defect disturbing the remethylation of homocysteine to methionine (< 200 reported …

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

M Huemer, R Mulder-bleile, P Burda… - Journal of Inherited …, 2016 - search.proquest.com
Background Severe methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare
inborn defect disturbing the remethylation of homocysteine to methionine (< 200 reported …
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[HTML][HTML] Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

M Huemer, R Mulder-Bleile, P Burda… - Journal of inherited …, 2016 - ncbi.nlm.nih.gov
Background Severe methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare (<
200 reported cases) inborn defect of the remethylation of homocysteine to methionine. This …

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

M Huemer, R Mulder-Bleile, P Burda, DS Froese… - 2016 - opus.bibliothek.uni-augsburg.de
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methylenetetrahydrofolate reductase (MTHFR) deficiency Deutsch Login Open Access Home …

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

M Huemer, R Mulder‐Bleile, P Burda… - Journal of Inherited …, 2016 - Wiley Online Library
Background Severe methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare
inborn defect disturbing the remethylation of homocysteine to methionine (< 200 reported …

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

M Huemer, R Mulder-Bleile, P Burda… - JOURNAL OF …, 2016 - pure.pmu.ac.at
Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10
methylenetetrahydrofolate reductase (MTHFR) deficiency — PMU Forschungsportal Zur …