S. Tey Et Al. , "Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family," NEUROGENETICS , vol.20, no.3, pp.117-127, 2019
Tey, S. Et Al. 2019. Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family. NEUROGENETICS , vol.20, no.3 , 117-127.
Tey, S., Shahrizaila, N., Drew, A. P., Samulong, S., Goh, K., BATTALOĞLU, E., ... Atkinson, D.(2019). Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family. NEUROGENETICS , vol.20, no.3, 117-127.
Tey, Shelisa Et Al. "Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family," NEUROGENETICS , vol.20, no.3, 117-127, 2019
Tey, Shelisa Et Al. "Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family." NEUROGENETICS , vol.20, no.3, pp.117-127, 2019
Tey, S. Et Al. (2019) . "Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family." NEUROGENETICS , vol.20, no.3, pp.117-127.
@article{article, author={Shelisa Tey Et Al. }, title={Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family}, journal={NEUROGENETICS}, year=2019, pages={117-127} }