FBN2 pathogenic mutation in congenital contractural arachnodactyly with severe skeletal manifestations.

Huang Y, Fang X, Ma L, Zhang J, Wang C, Gao T, Peng D

Open source

DOI
10.1016/j.ymgmr.2025.101193
Published
2025 Mar
Container
Molecular genetics and metabolism reports
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1016/j.ymgmr.2025.101193,
  title = {FBN2 pathogenic mutation in congenital contractural arachnodactyly with severe skeletal manifestations.},
  author = {Huang Y and Fang X and Ma L and Zhang J and Wang C and Gao T and Peng D},
  year = {2025},
  journal = {Molecular genetics and metabolism reports},
  doi = {10.1016/j.ymgmr.2025.101193},
  url = {https://doi.org/10.1016/j.ymgmr.2025.101193}
}

RIS

TY  - JOUR
TI  - FBN2 pathogenic mutation in congenital contractural arachnodactyly with severe skeletal manifestations.
AU  - Huang Y
AU  - Fang X
AU  - Ma L
AU  - Zhang J
AU  - Wang C
AU  - Gao T
AU  - Peng D
PY  - 2025
JO  - Molecular genetics and metabolism reports
DO  - 10.1016/j.ymgmr.2025.101193
UR  - https://doi.org/10.1016/j.ymgmr.2025.101193
ER  -

APA

Y, H., X, F., L, M., J, Z., C, W., T, G., & D, P. (2025). FBN2 pathogenic mutation in congenital contractural arachnodactyly with severe skeletal manifestations.. Molecular genetics and metabolism reports. https://doi.org/10.1016/j.ymgmr.2025.101193

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