Defective lysosomal release of vitamin B12 (cblF): A hereditary cobalamin metabolic disorder associated with sudden death
VE Shih, SM Axel, JC Tewksbury… - American journal of …, 1989 - Wiley Online Library
Here we report on a girl who presented with failure to thrive, developmental delay, minor
facial anomalies, stomatitis, skin rashes, macrocytosis, mild homocystinemia‐(uria), and …
facial anomalies, stomatitis, skin rashes, macrocytosis, mild homocystinemia‐(uria), and …
Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden death
VE Shih, SM Axel, JC Tewksbury… - … journal of medical …, 1989 - pubmed.ncbi.nlm.nih.gov
Here we report on a girl who presented with failure to thrive, developmental delay, minor
facial anomalies, stomatitis, skin rashes, macrocytosis, mild homocystinemia (uria), and …
facial anomalies, stomatitis, skin rashes, macrocytosis, mild homocystinemia (uria), and …
Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden death.
VE Shih, SM Axel, JC Tewksbury… - American Journal of …, 1989 - europepmc.org
Here we report on a girl who presented with failure to thrive, developmental delay, minor
facial anomalies, stomatitis, skin rashes, macrocytosis, mild homocystinemia (uria), and …
facial anomalies, stomatitis, skin rashes, macrocytosis, mild homocystinemia (uria), and …
[引用][C] Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden death
VE SHIH, SM AXEL, JC TEWKSBURY… - American journal of …, 1989 - pascal-francis.inist.fr
Defective lysosomal release of vitamin B12(cb1F): a hereditary cobalamin metabolic
disorder associated with sudden death CNRS Inist Pascal-Francis CNRS Pascal and …
disorder associated with sudden death CNRS Inist Pascal-Francis CNRS Pascal and …