Edvardson, S., Tian, G., Cullen, H., Vanyai, H., Ngo, L., Bhat, S., . . . Elpeleg, O. (2016). Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway. Hum Mol Genet.
Styl ChicagoEdvardson, Shimon, et al. "Infantile Neurodegenerative Disorder Associated With Mutations in TBCD, an Essential Gene in the Tubulin Heterodimer Assembly Pathway." Hum Mol Genet 2016.
Citace podle MLAEdvardson, Shimon, et al. "Infantile Neurodegenerative Disorder Associated With Mutations in TBCD, an Essential Gene in the Tubulin Heterodimer Assembly Pathway." Hum Mol Genet 2016.
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