Topcu, M. Et Al. 2017. Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family Member. MOLECULAR DIAGNOSIS & THERAPY , vol.21, no.6 , 643-651.

Topcu, M., Aktas, D., Oztoprak, M., Mungan, N. O., YÜCE, A., & ALİKAŞİFOĞLU, M., (2017). Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family Member. MOLECULAR DIAGNOSIS & THERAPY , vol.21, no.6, 643-651.

Topcu, Meral Et Al. "Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family Member," MOLECULAR DIAGNOSIS & THERAPY , vol.21, no.6, 643-651, 2017

Topcu, Meral Et Al. "Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family Member." MOLECULAR DIAGNOSIS & THERAPY , vol.21, no.6, pp.643-651, 2017

Topcu, M. Et Al. (2017) . "Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family Member." MOLECULAR DIAGNOSIS & THERAPY , vol.21, no.6, pp.643-651.

@article{article, author={Meral Topcu Et Al. }, title={Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family Member}, journal={MOLECULAR DIAGNOSIS & THERAPY}, year=2017, pages={643-651} }