QuickView for AP4M1;jsessionid=45E46964C1CD47C8457ADDD2C8FEDDE8 (gene)

1. Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epi…
2. Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three f…
3. Severe congenital microcephaly with AP4M1 mutation, a case report.
4. AP4M1 is abnormally expressed in oxygen-glucose deprived hippocampal neurons.
5. A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4…

There were no clinical trials for AP4M1;jsessionid=45E46964C1CD47C8457ADDD2C8FEDDE8