Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability.
- DOI
- 10.1136/jmedgenet-2017-104620
- Published
- 2018 Jan
- Container
- Journal of medical genetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1136/jmedgenet-2017-104620,
title = {Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability.},
author = {Hamilton MJ and Caswell RC and Canham N and Cole T and Firth HV and Foulds N and Heimdal K and Hobson E and Houge G and Joss S and Kumar D and Lampe AK and Maystadt I and McKay V and Metcalfe K and Newbury-Ecob R and Park SM and Robert L and Rustad CF and Wakeling E and Wilkie AOM and Study TDDD and Twigg SRF and Suri M},
year = {2018},
journal = {Journal of medical genetics},
doi = {10.1136/jmedgenet-2017-104620},
url = {https://doi.org/10.1136/jmedgenet-2017-104620}
}RIS
TY - JOUR TI - Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability. AU - Hamilton MJ AU - Caswell RC AU - Canham N AU - Cole T AU - Firth HV AU - Foulds N AU - Heimdal K AU - Hobson E AU - Houge G AU - Joss S AU - Kumar D AU - Lampe AK AU - Maystadt I AU - McKay V AU - Metcalfe K AU - Newbury-Ecob R AU - Park SM AU - Robert L AU - Rustad CF AU - Wakeling E AU - Wilkie AOM AU - Study TDDD AU - Twigg SRF AU - Suri M PY - 2018 JO - Journal of medical genetics DO - 10.1136/jmedgenet-2017-104620 UR - https://doi.org/10.1136/jmedgenet-2017-104620 ER -
APA
MJ, H., RC, C., N, C., T, C., HV, F., N, F., K, H., E, H., G, H., S, J., D, K., AK, L., I, M., V, M., K, M., R, N., SM, P., L, R., CF, R., E, W., AOM, W., TDDD, S., SRF, T., & M, S. (2018). Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability.. Journal of medical genetics. https://doi.org/10.1136/jmedgenet-2017-104620
Source records
- pubmed · retrieved 2026-09-27T14:04:28.999Z