p.Arg69Trp in <i>RNASEH2C</i> is a founder variant in three Indian families with Aicardi–Goutières syndrome
- DOI
- 10.1002/ajmg.a.38522
- Published
- 2017-11-17
- Container
- American Journal of Medical Genetics Part A
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/ajmg.a.38522,
title = {p.Arg69Trp in <i>RNASEH2C</i> is a founder variant in three Indian families with Aicardi–Goutières syndrome},
author = {Malavika Hebbar and Anil Kanthi and Aroor Shrikiran and Snehal Patil and Mamta Muranjan and Febi Francis and Vishnu Bhat B and Katta M Girisha and Anju Shukla},
year = {2017},
journal = {American Journal of Medical Genetics Part A},
doi = {10.1002/ajmg.a.38522},
url = {https://doi.org/10.1002/ajmg.a.38522}
}RIS
TY - JOUR TI - p.Arg69Trp in <i>RNASEH2C</i> is a founder variant in three Indian families with Aicardi–Goutières syndrome AU - Malavika Hebbar AU - Anil Kanthi AU - Aroor Shrikiran AU - Snehal Patil AU - Mamta Muranjan AU - Febi Francis AU - Vishnu Bhat B AU - Katta M Girisha AU - Anju Shukla PY - 2017 JO - American Journal of Medical Genetics Part A DO - 10.1002/ajmg.a.38522 UR - https://doi.org/10.1002/ajmg.a.38522 ER -
APA
Hebbar, M., Kanthi, A., Shrikiran, A., Patil, S., Muranjan, M., Francis, F., B, V. B., Girisha, K. M., & Shukla, A. (2017). p.Arg69Trp in <i>RNASEH2C</i> is a founder variant in three Indian families with Aicardi–Goutières syndrome. American Journal of Medical Genetics Part A. https://doi.org/10.1002/ajmg.a.38522
Source records
- crossref · retrieved 2026-09-26T17:48:35.374Z