AP4B1 hypomorphic variants cause autosomal recessive adult-onset ataxia.
Sabbagh Q, Poblete NH, Angelini C, Hersent C, Benkirane M, Pointaux M, Larrieu L, Castrioto A, Deberge L, Fluchère F, Ramond F, Lesca G, Koenig M, Goizet C.
Sabbagh Q, et al. Among authors: koenig m.
J Neurol. 2025 Jan 17;272(2):154. doi: 10.1007/s00415-025-12889-5.
J Neurol. 2025.
PMID: 39821477
Free PMC article.
No abstract available.