APA

Saha B., Lessel D., Nampoothiri S., Rao A. S., Hisama F. M., Peter D., Bennett C., Nürnberg G., Nürnberg P., Martin G. M., Kubisch C. & Oshima J. (2013). Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry. : Molecular genetics & genomic medicine.

Chicago

Saha Bidisha, Lessel Davor, Nampoothiri Sheela, Rao Anuradha S, Hisama Fuki M, Peter Dincy, Bennett Chris, Nürnberg Gudrun, Nürnberg Peter, Martin George M, Kubisch Christian and Oshima Junko. 2013. Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry. : Molecular genetics & genomic medicine.

Harvard

Saha B., Lessel D., Nampoothiri S., Rao A. S., Hisama F. M., Peter D., Bennett C., Nürnberg G., Nürnberg P., Martin G. M., Kubisch C. and Oshima J. (2013). Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry. : Molecular genetics & genomic medicine.

MLA

Saha Bidisha, Lessel Davor, Nampoothiri Sheela, Rao Anuradha S, Hisama Fuki M, Peter Dincy, Bennett Chris, Nürnberg Gudrun, Nürnberg Peter, Martin George M, Kubisch Christian and Oshima Junko. Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry. : Molecular genetics & genomic medicine. 2013.