APA

Liew W. K. M., Ben-Omran T., Darras B. T., Prabhu S. P., De Vivo D. C., Vatta M., Yang Y., Eng C. M. & Chung W. K. (20130829). Clinical application of whole-exome sequencing: a novel autosomal recessive spastic ataxia of Charlevoix-Saguenay sequence variation in a child with ataxia. : JAMA neurology.

Chicago

Liew Wendy K M, Ben-Omran Tawfeg, Darras Basil T, Prabhu Sanjay P, De Vivo Darryl C, Vatta Matteo, Yang Yaping, Eng Christine M and Chung Wendy K. 20130829. Clinical application of whole-exome sequencing: a novel autosomal recessive spastic ataxia of Charlevoix-Saguenay sequence variation in a child with ataxia. : JAMA neurology.

Harvard

Liew W. K. M., Ben-Omran T., Darras B. T., Prabhu S. P., De Vivo D. C., Vatta M., Yang Y., Eng C. M. and Chung W. K. (20130829). Clinical application of whole-exome sequencing: a novel autosomal recessive spastic ataxia of Charlevoix-Saguenay sequence variation in a child with ataxia. : JAMA neurology.

MLA

Liew Wendy K M, Ben-Omran Tawfeg, Darras Basil T, Prabhu Sanjay P, De Vivo Darryl C, Vatta Matteo, Yang Yaping, Eng Christine M and Chung Wendy K. Clinical application of whole-exome sequencing: a novel autosomal recessive spastic ataxia of Charlevoix-Saguenay sequence variation in a child with ataxia. : JAMA neurology. 20130829.