Whole-body MRI evaluation in neurofibromatosis type 1 patients younger than 3 years old and the genetic contribution to disease progression.
- DOI
- 10.1186/s13023-022-02174-3
- Published
- 2022 Jan 29
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-022-02174-3,
title = {Whole-body MRI evaluation in neurofibromatosis type 1 patients younger than 3 years old and the genetic contribution to disease progression.},
author = {Kang E and Kim YM and Choi Y and Lee Y and Kim J and Choi IH and Yoo HW and Yoon HM and Lee BH},
year = {2022},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-022-02174-3},
url = {https://doi.org/10.1186/s13023-022-02174-3}
}RIS
TY - JOUR TI - Whole-body MRI evaluation in neurofibromatosis type 1 patients younger than 3 years old and the genetic contribution to disease progression. AU - Kang E AU - Kim YM AU - Choi Y AU - Lee Y AU - Kim J AU - Choi IH AU - Yoo HW AU - Yoon HM AU - Lee BH PY - 2022 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-022-02174-3 UR - https://doi.org/10.1186/s13023-022-02174-3 ER -
APA
E, K., YM, K., Y, C., Y, L., J, K., IH, C., HW, Y., HM, Y., & BH, L. (2022). Whole-body MRI evaluation in neurofibromatosis type 1 patients younger than 3 years old and the genetic contribution to disease progression.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-022-02174-3
Source records
- pubmed · retrieved 2026-09-26T23:58:16.969Z