<scp>CHEDDA</scp> syndrome is an underrecognized neurodevelopmental disorder with a highly restricted <scp> <i>ATN1</i> </scp> mutation spectrum

Elizabeth E. Palmer, Chloe Whitton, Mais O. Hashem, Robin D. Clark, Subhadra Ramanathan, Lois J. Starr, Danita Velasco, John Karl De Dios, Emily Singh, Valerie Cormier‐Daire, Maya Chopra, Lance H. Rodan, Christoffer Nellaker, Shenela Lakhani, Eric J. Mallack, Karin Panzer, Alpa Sidhu, Ingrid M. Wentzensen, Didier Lacombe, Vincent Michaud, Fowzan S. Alkuraya

Open source

DOI: 10.1111/cge.14022
Published: 2021-07-13
Container: Clinical Genetics
Publisher: Wiley
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1111/cge.14022,
  title = {<scp>CHEDDA</scp>
                    syndrome is an underrecognized neurodevelopmental disorder with a highly restricted
                    <scp>
                      <i>ATN1</i>
                    </scp>
                    mutation spectrum},
  author = {Elizabeth E. Palmer and Chloe Whitton and Mais O. Hashem and Robin D. Clark and Subhadra Ramanathan and Lois J. Starr and Danita Velasco and John Karl De Dios and Emily Singh and Valerie Cormier‐Daire and Maya Chopra and Lance H. Rodan and Christoffer Nellaker and Shenela Lakhani and Eric J. Mallack and Karin Panzer and Alpa Sidhu and Ingrid M. Wentzensen and Didier Lacombe and Vincent Michaud and Fowzan S. Alkuraya},
  year = {2021},
  journal = {Clinical Genetics},
  doi = {10.1111/cge.14022},
  url = {https://doi.org/10.1111/cge.14022}
}

RIS

TY  - JOUR
TI  - <scp>CHEDDA</scp>
                    syndrome is an underrecognized neurodevelopmental disorder with a highly restricted
                    <scp>
                      <i>ATN1</i>
                    </scp>
                    mutation spectrum
AU  - Elizabeth E. Palmer
AU  - Chloe Whitton
AU  - Mais O. Hashem
AU  - Robin D. Clark
AU  - Subhadra Ramanathan
AU  - Lois J. Starr
AU  - Danita Velasco
AU  - John Karl De Dios
AU  - Emily Singh
AU  - Valerie Cormier‐Daire
AU  - Maya Chopra
AU  - Lance H. Rodan
AU  - Christoffer Nellaker
AU  - Shenela Lakhani
AU  - Eric J. Mallack
AU  - Karin Panzer
AU  - Alpa Sidhu
AU  - Ingrid M. Wentzensen
AU  - Didier Lacombe
AU  - Vincent Michaud
AU  - Fowzan S. Alkuraya
PY  - 2021
JO  - Clinical Genetics
DO  - 10.1111/cge.14022
UR  - https://doi.org/10.1111/cge.14022
ER  -

APA

Palmer, E. E., Whitton, C., Hashem, M. O., Clark, R. D., Ramanathan, S., Starr, L. J., Velasco, D., Dios, J. K. D., Singh, E., Cormier‐Daire, V., Chopra, M., Rodan, L. H., Nellaker, C., Lakhani, S., Mallack, E. J., Panzer, K., Sidhu, A., Wentzensen, I. M., Lacombe, D., Michaud, V., & Alkuraya, F. S. (2021). <scp>CHEDDA</scp> syndrome is an underrecognized neurodevelopmental disorder with a highly restricted <scp> <i>ATN1</i> </scp> mutation spectrum. Clinical Genetics. https://doi.org/10.1111/cge.14022

Source records

crossref · retrieved 2026-09-25T03:40:32.369Z