Frequency of de novo variants and parental mosaicism in families with inactivating PTH/PTHrP signaling disorder type 2
- DOI
- 10.3389/fendo.2022.1055431
- Published
- 2023-01-04
- Container
- Frontiers in Endocrinology
- Publisher
- Frontiers Media SA
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.3389/fendo.2022.1055431,
title = {Frequency of de novo variants and parental mosaicism in families with inactivating PTH/PTHrP signaling disorder type 2},
author = {Yerai Vado and Arrate Pereda and Africa Manero-Azua and Unknown and Guiomar Perez de Nanclares},
year = {2023},
journal = {Frontiers in Endocrinology},
doi = {10.3389/fendo.2022.1055431},
url = {https://doi.org/10.3389/fendo.2022.1055431}
}RIS
TY - JOUR TI - Frequency of de novo variants and parental mosaicism in families with inactivating PTH/PTHrP signaling disorder type 2 AU - Yerai Vado AU - Arrate Pereda AU - Africa Manero-Azua AU - Unknown AU - Guiomar Perez de Nanclares PY - 2023 JO - Frontiers in Endocrinology DO - 10.3389/fendo.2022.1055431 UR - https://doi.org/10.3389/fendo.2022.1055431 ER -
APA
Vado, Y., Pereda, A., Manero-Azua, A., Unknown, & Nanclares, G. P. D. (2023). Frequency of de novo variants and parental mosaicism in families with inactivating PTH/PTHrP signaling disorder type 2. Frontiers in Endocrinology. https://doi.org/10.3389/fendo.2022.1055431
Source records
- crossref · retrieved 2026-09-25T12:25:28.968Z