Melatonin receptor 1A variants as genetic cause of idiopathic osteoporosis

Bisikirska, B., Labella, R., Cuesta-Dominguez, A., Luo, N., De Angelis, J., Mosialou, I., Lin, C.-S., Beck, D., Lata, S., Shyu, P. T., McMahon, D. J., Guo, E., Hagen, J., Chung, W. K., Shane, E., Cohen, A., & Kousteni, S. (2024). Melatonin receptor 1A variants as genetic cause of idiopathic osteoporosis. Science Translational Medicine, 16(769). https://doi.org/10.1126/scitranslmed.adj0085
Authors:
Brygida Bisikirska
Rossella Labella
Alvaro Cuesta-Dominguez
Na Luo
Jessica De Angelis
Ioanna Mosialou
Chyuan-Sheng Lin
David Beck
Sneh Lata
Peter Timothy Shyu
Donald J McMahon
Edward Guo
Jacob Hagen
Wendy K Chung
Elizabeth Shane
Adi Cohen
Stavroula Kousteni
Affiliated Authors:
Brygida Bisikirska
Rossella Labella
Alvaro Cuesta-Dominguez
Na Luo
Jessica De Angelis
Ioanna Mosialou
Chyuan-Sheng Lin
Sneh Lata
Peter Timothy Shyu
Donald J McMahon
Edward Guo
Jacob Hagen
Wendy K Chung
Elizabeth Shane
Adi Cohen
Stavroula Kousteni
Subjects:
Publication Type:
Article
Unique ID:
10.1126/scitranslmed.adj0085
PMID:
Publication Date:
Data Source:
PubMed

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