Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locus

Haematologica. 2020 Dec 1;105(12):2883-2886. doi: 10.3324/haematol.2020.258533.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anemia, Sideroblastic* / genetics
  • Genetic Diseases, X-Linked*
  • Humans
  • Mitochondrial Membrane Transport Proteins / genetics
  • Uniparental Disomy / genetics

Substances

  • Mitochondrial Membrane Transport Proteins
  • Slc25a38 protein, human

Grants and funding

Funding: this work was supported by an EHA Junior Research Grant to Immacolata Andolfo (3978026), and by a Bando Star Linea 1 - Junior Principal Ivestigator Grants - COINOR, Università degli Studi di Napoli ‘Federico II’ to Roberta Russo. The authors also thank the parents of the patient for granting their permission for the case to be communicated to the scientific community.