Phenotypic expression of swallowing function in Niemann–Pick disease type C1

Beth I. Solomon, Andrea M. Muñoz, Ninet Sinaii, Nicole M. Farhat, Andrew C. Smith, Simona Bianconi, An Dang Do, Michael C. Backman, Leonza Machielse, Forbes D. Porter

Open source

DOI: 10.1186/s13023-022-02472-w
Published: 2022-09-05
Container: Orphanet Journal of Rare Diseases
Publisher: Springer Science and Business Media LLC
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1186/s13023-022-02472-w,
  title = {Phenotypic expression of swallowing function in Niemann–Pick disease type C1},
  author = {Beth I. Solomon and Andrea M. Muñoz and Ninet Sinaii and Nicole M. Farhat and Andrew C. Smith and Simona Bianconi and An Dang Do and Michael C. Backman and Leonza Machielse and Forbes D. Porter},
  year = {2022},
  journal = {Orphanet Journal of Rare Diseases},
  doi = {10.1186/s13023-022-02472-w},
  url = {https://doi.org/10.1186/s13023-022-02472-w}
}

RIS

TY  - JOUR
TI  - Phenotypic expression of swallowing function in Niemann–Pick disease type C1
AU  - Beth I. Solomon
AU  - Andrea M. Muñoz
AU  - Ninet Sinaii
AU  - Nicole M. Farhat
AU  - Andrew C. Smith
AU  - Simona Bianconi
AU  - An Dang Do
AU  - Michael C. Backman
AU  - Leonza Machielse
AU  - Forbes D. Porter
PY  - 2022
JO  - Orphanet Journal of Rare Diseases
DO  - 10.1186/s13023-022-02472-w
UR  - https://doi.org/10.1186/s13023-022-02472-w
ER  -

APA

Solomon, B. I., Muñoz, A. M., Sinaii, N., Farhat, N. M., Smith, A. C., Bianconi, S., Do, A. D., Backman, M. C., Machielse, L., & Porter, F. D. (2022). Phenotypic expression of swallowing function in Niemann–Pick disease type C1. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-022-02472-w

Source records

crossref · retrieved 2026-09-26T22:09:37.934Z