Search Results - Edvardson, S.

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    Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway

    Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway by Edvardson, S., Tian, G., Cullen, H., Vanyai, H., Ngo, L., Bhat, S., Aran, A., Daana, M., Da'amseh, N., Abu-Libdeh, B., Cowan, N., Heng, Julian, Elpeleg, O.

    Published 2016
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