A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia.
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ABSTRACT:
SUBMITTER: Svaton M
PROVIDER: S-EPMC7330012 | biostudies-literature | 2020 Jun
REPOSITORIES: biostudies-literature
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A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia.
Svaton Michael M Skvarova Kramarzova Karolina K Kanderova Veronika V Mancikova Andrea A Smisek Petr P Jesina Pavel P Krijt Jakub J Stiburkova Blanka B Dobrovolny Robert R Sokolova Jitka J Bakardjieva-Mihaylova Violeta V Vodickova Elena E Rackova Marketa M Stuchly Jan J Kalina Tomas T Stary Jan J Trka Jan J Fronkova Eva E Kozich Viktor V
Blood 20200601 26
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