Author:
Manoochehri Jamal,Goodarzi Hamed Reza,Tabei Seyed Mohammad Bagher
Publisher
Springer Science and Business Media LLC
Reference19 articles.
1. De Pace R., Skirzewski M., Damme M., Mattera R., Mercurio J., Foster A. M. et al. 2018 Altered distribution of ATG9A and accumulation of axonal aggregates in neurons from a mouse model of AP-4 deficiency syndrome. PLoS Genet. 14, e1007363.
2. Ebrahimi-Fakhari D., Behne R., Davies A. K. and Hirst J. 1993 AP-4-Associated hereditary spastic paraplegia (ed. M. P. Adam, H. H. Ardinger, R. A. Pagon, S. E. Wallace, L. J. H. Bean, G. Mirzaa and A. Amemiya). Seattle.
3. Faghihi F., Khamirani H. J., Zoghi S., Kamal N., Yeganehe S. B., Dianatpour M. et al. 2022 Phenotypic spectrum of autosomal recessive keratitis-ichthyosis-deafness syndrome (KIDAR) due to mutations in AP1B1. Eur. J. Med. Genet. 65, 104449.
4. Fink J. K. 2013 Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms. Acta Neuropathol. 126, 307–328.
5. Hirst J., Bright N. A., Rous B. and Robinson M. S. 1999 Characterization of a fourth adaptor-related protein complex. Mol. Biol. Cell 10, 2787–2802.