Title : ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies - Lemire_2021_Am.J.Hum.Genet__ |
Author(s) :
Lemire G , Ito YA , Marshall AE , Chrestian N , Stanley V , Brady L , Tarnopolsky M , Curry CJ , Hartley T , Mears W , Derksen A , Rioux N , Laflamme N , Hutchison HT , Pais LS , Zaki MS , Sultan T , Dane AD , Gleeson JG , Vaz FM , Kernohan KD , Bernard G , Boycott KM |
Ref :
American Journal of Human Genetics , : , 2021 |
Abstract : Lemire_2021_Am.J.Hum.Genet__ |
ESTHER : Lemire_2021_Am.J.Hum.Genet__ |
PubMedSearch : Lemire_2021_Am.J.Hum.Genet__ |
PubMedID: 34587489 |
Gene_locus related to this paper:
human-ABHD16A |