APA

Cortese A., Zhu Y., Rebelo A. P., Negri S., Courel S., Abreu L., Bacon C. J., Bai Y., Bis-Brewer D. M., Bugiardini E., Buglo E., Danzi M. C., Feely S. M. E., Athanasiou-Fragkouli A., Haridy N. A., Isasi R., Khan A., Laurà M., Magri S., Pipis M., Pisciotta C., Powell E., Rossor A. M., Saveri P., Sowden J. E., Tozza S., Vandrovcova J., Dallman J., Grignani E., Marchioni E., Scherer S. S., Tang B., Lin Z., Al-Ajmi A., Schüle R., Synofzik M., Maisonobe T., Stojkovic T., Auer-Grumbach M., Abdelhamed M. A., Hamed S. A., Zhang R., Manganelli F., Santoro L., Taroni F., Pareyson D., Houlden H., Herrmann D. N., Reilly M. M., Shy M. E., Zhai R. G. & Zuchner S. (20200803). Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. : Nature genetics.

Chicago

Cortese Andrea, Zhu Yi, Rebelo Adriana P, Negri Sara, Courel Steve, Abreu Lisa, Bacon Chelsea J, Bai Yunhong, Bis-Brewer Dana M, Bugiardini Enrico, Buglo Elena, Danzi Matt C, Feely Shawna M E, Athanasiou-Fragkouli Alkyoni, Haridy Nourelhoda A, Isasi Rosario, Khan Alaa, Laurà Matilde, Magri Stefania, Pipis Menelaos, Pisciotta Chiara, Powell Eric, Rossor Alexander M, Saveri Paola, Sowden Janet E, Tozza Stefano, Vandrovcova Jana, Dallman Julia, Grignani Elena, Marchioni Enrico, Scherer Steven S, Tang Beisha, Lin Zhiqiang, Al-Ajmi Abdullah, Schüle Rebecca, Synofzik Matthis, Maisonobe Thierry, Stojkovic Tanya, Auer-Grumbach Michaela, Abdelhamed Mohamed A, Hamed Sherifa A, Zhang Ruxu, Manganelli Fiore, Santoro Lucio, Taroni Franco, Pareyson Davide, Houlden Henry, Herrmann David N, Reilly Mary M, Shy Michael E, Zhai R Grace and Zuchner Stephan. 20200803. Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. : Nature genetics.

Harvard

Cortese A., Zhu Y., Rebelo A. P., Negri S., Courel S., Abreu L., Bacon C. J., Bai Y., Bis-Brewer D. M., Bugiardini E., Buglo E., Danzi M. C., Feely S. M. E., Athanasiou-Fragkouli A., Haridy N. A., Isasi R., Khan A., Laurà M., Magri S., Pipis M., Pisciotta C., Powell E., Rossor A. M., Saveri P., Sowden J. E., Tozza S., Vandrovcova J., Dallman J., Grignani E., Marchioni E., Scherer S. S., Tang B., Lin Z., Al-Ajmi A., Schüle R., Synofzik M., Maisonobe T., Stojkovic T., Auer-Grumbach M., Abdelhamed M. A., Hamed S. A., Zhang R., Manganelli F., Santoro L., Taroni F., Pareyson D., Houlden H., Herrmann D. N., Reilly M. M., Shy M. E., Zhai R. G. and Zuchner S. (20200803). Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. : Nature genetics.

MLA

Cortese Andrea, Zhu Yi, Rebelo Adriana P, Negri Sara, Courel Steve, Abreu Lisa, Bacon Chelsea J, Bai Yunhong, Bis-Brewer Dana M, Bugiardini Enrico, Buglo Elena, Danzi Matt C, Feely Shawna M E, Athanasiou-Fragkouli Alkyoni, Haridy Nourelhoda A, Isasi Rosario, Khan Alaa, Laurà Matilde, Magri Stefania, Pipis Menelaos, Pisciotta Chiara, Powell Eric, Rossor Alexander M, Saveri Paola, Sowden Janet E, Tozza Stefano, Vandrovcova Jana, Dallman Julia, Grignani Elena, Marchioni Enrico, Scherer Steven S, Tang Beisha, Lin Zhiqiang, Al-Ajmi Abdullah, Schüle Rebecca, Synofzik Matthis, Maisonobe Thierry, Stojkovic Tanya, Auer-Grumbach Michaela, Abdelhamed Mohamed A, Hamed Sherifa A, Zhang Ruxu, Manganelli Fiore, Santoro Lucio, Taroni Franco, Pareyson Davide, Houlden Henry, Herrmann David N, Reilly Mary M, Shy Michael E, Zhai R Grace and Zuchner Stephan. Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. : Nature genetics. 20200803.