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ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies

Research output: Contribution to journal › Article › Academic › peer-review

Original language	English
Pages (from-to)	2017-2023
Number of pages	7
Journal	American journal of human genetics
Volume	108
Issue number	10
DOIs	https://doi.org/10.1016/j.ajhg.2021.09.005
Publication status	Published - 7 Oct 2021

ABHD16A, hereditary spastic paraplegia, intellectual disability, lysophosphatidylserine

ID: 20117375