Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder
Raman Kumar, Mark Corbett, Nicholas Smith, Lachlan Jolly, Chuan Tan, Damien Keating, Michael Duffield, Toshihiko Utsumi, Koko Moriya, Katherine Smith, Alexander Hoischen, Kym Abbott, Michael Harbord, Alison Compton, Joshua Woenig, Peer Arts, Michael Kwint, Nienke Wieskamp, Sabine Gijsen, Joris Veltman
Research output: Contribution to journal › Article › peer-review
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