Unknown

Dataset Information

0

A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia.


ABSTRACT:

SUBMITTER: Svaton M 

PROVIDER: S-EPMC7330012 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC3035706 | biostudies-literature
| S-EPMC9794768 | biostudies-literature
| S-EPMC9822521 | biostudies-literature
| S-EPMC3046546 | biostudies-literature
| S-EPMC3831518 | biostudies-literature
| S-EPMC6054684 | biostudies-literature
| S-EPMC2812009 | biostudies-literature
| S-EPMC3835300 | biostudies-literature
| S-EPMC2858590 | biostudies-literature
| S-EPMC8895901 | biostudies-literature