Neurologic phenotypes associated with <i>COL4A1</i> / <i>2</i> mutations

Sara Zagaglia, Christina Selch, Jelena Radic Nisevic, Davide Mei, Zuzanna Michalak, Laura Hernandez-Hernandez, S. Krithika, Katharina Vezyroglou, Sophia M. Varadkar, Alexander Pepler, Saskia Biskup, Miguel Leão, Jutta Gärtner, Andreas Merkenschlager, Michaela Jaksch, Rikke S. Møller, Elena Gardella, Britta Schlott Kristiansen, Lars Kjærsgaard Hansen, Maria Stella Vari, Katherine L. Helbig, Sonal Desai, Constance L. Smith-Hicks, Naomi Hino-Fukuyo, Tiina Talvik, Rael Laugesaar, Pilvi Ilves, Katrin Õunap, Ingrid Körber, Till Hartlieb, Manfred Kudernatsch, Peter Winkler, Mareike Schimmel, Anette Hasse, Markus Knuf, Jan Heinemeyer, Christine Makowski, Sondhya Ghedia, Gopinath M. Subramanian, Pasquale Striano, Rhys H. Thomas, Caroline Micallef, Maria Thom, David J. Werring, Gerhard Josef Kluger, J. Helen Cross, Renzo Guerrini, Simona Balestrini, Sanjay M. Sisodiya

Open source

DOI
10.1212/wnl.0000000000006567
Published
2018-11-27
Container
Neurology
Publisher
Ovid Technologies (Wolters Kluwer Health)
Open access
unknown

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BibTeX

@article{allodium:10.1212/wnl.0000000000006567,
  title = {Neurologic phenotypes associated with
            <i>COL4A1</i>
            /
            <i>2</i>
            mutations},
  author = {Sara Zagaglia and Christina Selch and Jelena Radic Nisevic and Davide Mei and Zuzanna Michalak and Laura Hernandez-Hernandez and S. Krithika and Katharina Vezyroglou and Sophia M. Varadkar and Alexander Pepler and Saskia Biskup and Miguel Leão and Jutta Gärtner and Andreas Merkenschlager and Michaela Jaksch and Rikke S. Møller and Elena Gardella and Britta Schlott Kristiansen and Lars Kjærsgaard Hansen and Maria Stella Vari and Katherine L. Helbig and Sonal Desai and Constance L. Smith-Hicks and Naomi Hino-Fukuyo and Tiina Talvik and Rael Laugesaar and Pilvi Ilves and Katrin Õunap and Ingrid Körber and Till Hartlieb and Manfred Kudernatsch and Peter Winkler and Mareike Schimmel and Anette Hasse and Markus Knuf and Jan Heinemeyer and Christine Makowski and Sondhya Ghedia and Gopinath M. Subramanian and Pasquale Striano and Rhys H. Thomas and Caroline Micallef and Maria Thom and David J. Werring and Gerhard Josef Kluger and J. Helen Cross and Renzo Guerrini and Simona Balestrini and Sanjay M. Sisodiya},
  year = {2018},
  journal = {Neurology},
  doi = {10.1212/wnl.0000000000006567},
  url = {https://doi.org/10.1212/wnl.0000000000006567}
}

RIS

TY  - JOUR
TI  - Neurologic phenotypes associated with
            <i>COL4A1</i>
            /
            <i>2</i>
            mutations
AU  - Sara Zagaglia
AU  - Christina Selch
AU  - Jelena Radic Nisevic
AU  - Davide Mei
AU  - Zuzanna Michalak
AU  - Laura Hernandez-Hernandez
AU  - S. Krithika
AU  - Katharina Vezyroglou
AU  - Sophia M. Varadkar
AU  - Alexander Pepler
AU  - Saskia Biskup
AU  - Miguel Leão
AU  - Jutta Gärtner
AU  - Andreas Merkenschlager
AU  - Michaela Jaksch
AU  - Rikke S. Møller
AU  - Elena Gardella
AU  - Britta Schlott Kristiansen
AU  - Lars Kjærsgaard Hansen
AU  - Maria Stella Vari
AU  - Katherine L. Helbig
AU  - Sonal Desai
AU  - Constance L. Smith-Hicks
AU  - Naomi Hino-Fukuyo
AU  - Tiina Talvik
AU  - Rael Laugesaar
AU  - Pilvi Ilves
AU  - Katrin Õunap
AU  - Ingrid Körber
AU  - Till Hartlieb
AU  - Manfred Kudernatsch
AU  - Peter Winkler
AU  - Mareike Schimmel
AU  - Anette Hasse
AU  - Markus Knuf
AU  - Jan Heinemeyer
AU  - Christine Makowski
AU  - Sondhya Ghedia
AU  - Gopinath M. Subramanian
AU  - Pasquale Striano
AU  - Rhys H. Thomas
AU  - Caroline Micallef
AU  - Maria Thom
AU  - David J. Werring
AU  - Gerhard Josef Kluger
AU  - J. Helen Cross
AU  - Renzo Guerrini
AU  - Simona Balestrini
AU  - Sanjay M. Sisodiya
PY  - 2018
JO  - Neurology
DO  - 10.1212/wnl.0000000000006567
UR  - https://doi.org/10.1212/wnl.0000000000006567
ER  -

APA

Zagaglia, S., Selch, C., Nisevic, J. R., Mei, D., Michalak, Z., Hernandez-Hernandez, L., Krithika, S., Vezyroglou, K., Varadkar, S. M., Pepler, A., Biskup, S., Leão, M., Gärtner, J., Merkenschlager, A., Jaksch, M., Møller, R. S., Gardella, E., Kristiansen, B. S., Hansen, L. K., Vari, M. S., Helbig, K. L., Desai, S., Smith-Hicks, C. L., Hino-Fukuyo, N., Talvik, T., Laugesaar, R., Ilves, P., Õunap, K., Körber, I., Hartlieb, T., Kudernatsch, M., Winkler, P., Schimmel, M., Hasse, A., Knuf, M., Heinemeyer, J., Makowski, C., Ghedia, S., Subramanian, G. M., Striano, P., Thomas, R. H., Micallef, C., Thom, M., Werring, D. J., Kluger, G. J., Cross, J. H., Guerrini, R., Balestrini, S., & Sisodiya, S. M. (2018). Neurologic phenotypes associated with <i>COL4A1</i> / <i>2</i> mutations. Neurology. https://doi.org/10.1212/wnl.0000000000006567

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