Variation in <i>SIPA1L2</i> is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A

Feifei Tao, Gary W. Beecham, Adriana P. Rebelo, John Svaren, Susan H. Blanton, John J. Moran, Camila Lopez‐Anido, Jasper M. Morrow, Lisa Abreu, Devon Rizzo, Callyn A. Kirk, Xingyao Wu, Shawna Feely, Camiel Verhamme, Mario A. Saporta, David N. Herrmann, John W. Day, Charlotte J. Sumner, Thomas E. Lloyd, Jun Li, Sabrina W. Yum, Franco Taroni, Frank Baas, Byung‐Ok Choi, Davide Pareyson, Steven S. Scherer, Mary M. Reilly, Michael E. Shy, Stephan Züchner, Unknown

Open source

DOI: 10.1002/ana.25426
Published: 2019-02-28
Container: Annals of Neurology
Publisher: Wiley
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1002/ana.25426,
  title = {Variation in <i>SIPA1L2</i> is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A},
  author = {Feifei Tao and Gary W. Beecham and Adriana P. Rebelo and John Svaren and Susan H. Blanton and John J. Moran and Camila Lopez‐Anido and Jasper M. Morrow and Lisa Abreu and Devon Rizzo and Callyn A. Kirk and Xingyao Wu and Shawna Feely and Camiel Verhamme and Mario A. Saporta and David N. Herrmann and John W. Day and Charlotte J. Sumner and Thomas E. Lloyd and Jun Li and Sabrina W. Yum and Franco Taroni and Frank Baas and Byung‐Ok Choi and Davide Pareyson and Steven S. Scherer and Mary M. Reilly and Michael E. Shy and Stephan Züchner and Unknown},
  year = {2019},
  journal = {Annals of Neurology},
  doi = {10.1002/ana.25426},
  url = {https://doi.org/10.1002/ana.25426}
}

RIS

TY  - JOUR
TI  - Variation in <i>SIPA1L2</i> is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A
AU  - Feifei Tao
AU  - Gary W. Beecham
AU  - Adriana P. Rebelo
AU  - John Svaren
AU  - Susan H. Blanton
AU  - John J. Moran
AU  - Camila Lopez‐Anido
AU  - Jasper M. Morrow
AU  - Lisa Abreu
AU  - Devon Rizzo
AU  - Callyn A. Kirk
AU  - Xingyao Wu
AU  - Shawna Feely
AU  - Camiel Verhamme
AU  - Mario A. Saporta
AU  - David N. Herrmann
AU  - John W. Day
AU  - Charlotte J. Sumner
AU  - Thomas E. Lloyd
AU  - Jun Li
AU  - Sabrina W. Yum
AU  - Franco Taroni
AU  - Frank Baas
AU  - Byung‐Ok Choi
AU  - Davide Pareyson
AU  - Steven S. Scherer
AU  - Mary M. Reilly
AU  - Michael E. Shy
AU  - Stephan Züchner
AU  - Unknown
PY  - 2019
JO  - Annals of Neurology
DO  - 10.1002/ana.25426
UR  - https://doi.org/10.1002/ana.25426
ER  -

APA

Tao, F., Beecham, G. W., Rebelo, A. P., Svaren, J., Blanton, S. H., Moran, J. J., Lopez‐Anido, C., Morrow, J. M., Abreu, L., Rizzo, D., Kirk, C. A., Wu, X., Feely, S., Verhamme, C., Saporta, M. A., Herrmann, D. N., Day, J. W., Sumner, C. J., Lloyd, T. E., Li, J., Yum, S. W., Taroni, F., Baas, F., Choi, B., Pareyson, D., Scherer, S. S., Reilly, M. M., Shy, M. E., Züchner, S., & Unknown (2019). Variation in <i>SIPA1L2</i> is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A. Annals of Neurology. https://doi.org/10.1002/ana.25426

Source records

crossref · retrieved 2026-09-27T00:31:17.211Z