Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency.
- DOI
- 10.6065/apem.2346236.118
- Published
- 2024 Jun
- Container
- Annals of pediatric endocrinology & metabolism
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.6065/apem.2346236.118,
title = {Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency.},
author = {Kang J and Kim MJ and Yoo S and Cheon CK},
year = {2024},
journal = {Annals of pediatric endocrinology \& metabolism},
doi = {10.6065/apem.2346236.118},
url = {https://doi.org/10.6065/apem.2346236.118}
}RIS
TY - JOUR TI - Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency. AU - Kang J AU - Kim MJ AU - Yoo S AU - Cheon CK PY - 2024 JO - Annals of pediatric endocrinology & metabolism DO - 10.6065/apem.2346236.118 UR - https://doi.org/10.6065/apem.2346236.118 ER -
APA
J, K., MJ, K., S, Y., & CK, C. (2024). Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency.. Annals of pediatric endocrinology & metabolism. https://doi.org/10.6065/apem.2346236.118
Source records
- pubmed · retrieved 2026-09-27T09:09:21.777Z