Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity.
- DOI
- 10.3324/haematol.2018.199109
- Published
- 2018 Dec
- Container
- Haematologica
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3324/haematol.2018.199109,
title = {Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity.},
author = {Berhe S and Heeney MM and Campagna DR and Thompson JF and White EJ and Ross T and Peake RWA and Hanrahan JD and Rodriguez V and Renaud DL and Patnaik MS and Chang E and Bottomley SS and Fleming MD},
year = {2018},
journal = {Haematologica},
doi = {10.3324/haematol.2018.199109},
url = {https://doi.org/10.3324/haematol.2018.199109}
}RIS
TY - JOUR TI - Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity. AU - Berhe S AU - Heeney MM AU - Campagna DR AU - Thompson JF AU - White EJ AU - Ross T AU - Peake RWA AU - Hanrahan JD AU - Rodriguez V AU - Renaud DL AU - Patnaik MS AU - Chang E AU - Bottomley SS AU - Fleming MD PY - 2018 JO - Haematologica DO - 10.3324/haematol.2018.199109 UR - https://doi.org/10.3324/haematol.2018.199109 ER -
APA
S, B., MM, H., DR, C., JF, T., EJ, W., T, R., RWA, P., JD, H., V, R., DL, R., MS, P., E, C., SS, B., & MD, F. (2018). Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity.. Haematologica. https://doi.org/10.3324/haematol.2018.199109
Source records
- pubmed · retrieved 2026-09-27T00:21:09.918Z