A novel mutation in LMBRD1 causes the cblF defect of vitamin B12 metabolism in a Turkish patient
S Gailus, T Suormala, AG Malerczyk-Aktas… - Journal of inherited …, 2010 - Springer
In the cblF defect of vitamin B 12 (cobalamin) metabolism, cobalamin is trapped in
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
A novel mutation in LMBRD1 causes the cblF defect of vitamin B (12) metabolism in a Turkish patient
S Gailus, T Suormala, AG Malerczyk-Aktas… - Journal of Inherited …, 2010 - edoc.unibas.ch
In the cblF defect of vitamin B (12)(cobalamin) metabolism, cobalamin is trapped in
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
A novel mutation in LMBRD1 causes the cblF defect of vitamin B12 metabolism in a Turkish patient
S Gailus, T Suormala… - Journal of Inherited …, 2010 - search.proquest.com
In the cblF defect of vitamin B^ sub 12^(cobalamin) metabolism, cobalamin is trapped in
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
[引用][C] A novel mutation in LMBRD1 causes the cblF defect of vitamin B12 metabolism in a Turkish patient
S GAILUS, T SUORMALA… - Journal of inherited …, 2010 - pascal-francis.inist.fr
A novel mutation in LMBRD1 causes the cblF defect of vitamin B12 metabolism in a Turkish
patient CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases …
patient CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases …
A novel mutation in LMBRD1 causes the cblF defect of vitamin B (12) metabolism in a Turkish patient
S Gailus, T Suormala… - Journal of inherited …, 2010 - pubmed.ncbi.nlm.nih.gov
In the cblF defect of vitamin B (12)(cobalamin) metabolism, cobalamin is trapped in
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
A novel mutation in LMBRD1 causes the cblF defect of vitamin B12 metabolism in a Turkish patient
S Gailus, T Suormala… - Journal of Inherited …, 2010 - Wiley Online Library
In the cblF defect of vitamin B12 (cobalamin) metabolism, cobalamin is trapped in
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
A novel mutation in LMBRD1 causes the cblF defect of vitamin B12 metabolism in a Turkish patient
S Gailus, T Suormala, AG Malerczyk-Aktas… - Journal of Inherited …, 2010 - infona.pl
In the cblF defect of vitamin B12 (cobalamin) metabolism, cobalamin is trapped in
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
A novel mutation in LMBRD1 causes the cblF defect of vitamin B (12) metabolism in a Turkish patient.
S Gailus, T Suormala, AG Malerczyk-Aktas… - Journal of Inherited …, 2010 - europepmc.org
In the cblF defect of vitamin B (12)(cobalamin) metabolism, cobalamin is trapped in
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …
lysosomes. Consequently, cobalamin coenzyme synthesis is blocked, and cofactors for …