2020
Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy
Publication
Publication
| Additional Metadata | |
|---|---|
| doi.org/10.1007/s00401-020-02128-8, hdl.handle.net/1765/124560 | |
| VSNU Open Access deal | |
| Acta Neuropathologica | |
| Organisation | Department of Clinical Genetics |
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AlMuhaizea, M. (Mohammed), AlMass, R. (Rawan), AlHargan, A. (Aljouhra), AlBader, A. (Anoud), Medico Salsench, E. (Eva), Howaidi, J. (Jude), … Kaya, N. (Namik). (2020). Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy. Acta Neuropathologica. doi:10.1007/s00401-020-02128-8 |
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