Insights into severe 5, 10‐methylenetetrahydrofolate reductase deficiency: molecular genetic and enzymatic characterization of 76 patients

P Burda, A Schäfer, T Suormala, T Rummel… - Human …, 2015 - Wiley Online Library
Methylenetetrahydrofolate reductase (MTHFR) deficiency is the most common inherited
disorder of folate metabolism and causes severe hyperhomocysteinaemia. To better …
被引用次数：76 相关文章

Insights into severe 5, 10-methylenetetrahydrofolate reductase deficiency: molecular genetic and enzymatic characterization of 76 patients

P Burda, A Schäfer, T Suormala, T Rummel, C Bürer… - Human Mutation, 2015 - zora.uzh.ch
5, 10-Methylenetetrahydrofolate reductase (MTHFR) deficiency is the most common
inherited disorder of folate metabolism and causes severe hyperhomocysteinaemia. To …

Insights into severe 5, 10-methylenetetrahydrofolate reductase deficiency: molecular genetic and enzymatic characterization of 76 patients.

P Burda, A Schäfer, T Suormala, T Rummel… - Human …, 2015 - europepmc.org
5, 10-Methylenetetrahydrofolate reductase (MTHFR) deficiency is the most common
inherited disorder of folate metabolism and causes severe hyperhomocysteinaemia. To …

[引用][C] Insights into Severe 5, 10-Methylenetetrahydrofolate Reductase Deficiency: Molecular Genetic and Enzymatic Characterization of 76 Patients

P Burda, A Schäfer, T Suormala, T Rummel, C Bürer… - Human Mutation, 2015 - cir.nii.ac.jp
Insights into Severe 5,10-Methylenetetrahydrofolate Reductase Deficiency: Molecular Genetic
and Enzymatic Characterization of 76 Patients | CiNii Research CiNii 国立情報学研究所 学術 …

Insights into severe 5, 10-methylenetetrahydrofolate reductase deficiency: molecular genetic and enzymatic characterization of 76 patients

P Burda, A Schäfer, T Suormala… - Human …, 2015 - pubmed.ncbi.nlm.nih.gov
5, 10-Methylenetetrahydrofolate reductase (MTHFR) deficiency is the most common
inherited disorder of folate metabolism and causes severe hyperhomocysteinaemia. To …

Insights into severe 5, 10-methylenetetrahydrofolate reductase deficiency: molecular genetic and enzymatic characterization of 76 patients.

P Burda, A Schäfer, T Suormala, T Rummel, C Bürer… - Human mutation, 2015 - sonar.ch
English 5, 10-Methylenetetrahydrofolate reductase (MTHFR) deficiency is the most common
inherited disorder of folate metabolism and causes severe hyperhomocysteinaemia. To …

Insights into Severe 5, 10‐Methylenetetrahydrofolate Reductase Deficiency: Molecular Genetic and Enzymatic Characterization of 76 Patients

P Burda, A Schäfer, T Suormala, T Rummel, C Bürer… - Human Mutation, 2015 - infona.pl
5, 10‐Methylenetetrahydrofolate reductase (MTHFR) deficiency is the most common
inherited disorder of folate metabolism and causes severe hyperhomocysteinaemia. To …

Insights into severe 5, 10-methylenetetrahydrofolate reductase deficiency: molecular genetic and enzymatic characterization of 76 patients.

P Burda, A Schäfer, T Suormala, T Rummel, C Bürer… - Human mutation, 2015 - folia.unifr.ch
English 5, 10-Methylenetetrahydrofolate reductase (MTHFR) deficiency is the most common
inherited disorder of folate metabolism and causes severe hyperhomocysteinaemia. To …