Kernohan KD

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 :

PubMedSearch : Lemire_2021_Am.J.Hum.Genet__

PubMedID: 34587489

Gene_locus related to this paper: human-ABHD16A

Title : ATRX promotes gene expression by facilitating transcriptional elongation through guanine-rich coding regions - Levy_2015_Hum.Mol.Genet_24_1824

Author(s) : Levy MA , Kernohan KD , Jiang Y , Berube NG

Ref : Hum Mol Genet , 24 :1824 , 2015

Abstract :

PubMedSearch : Levy_2015_Hum.Mol.Genet_24_1824

PubMedID: 25452430

Kernohan KD

References (2)

1. ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies - Lemire_2021_Am.J.Hum.Genet__

2. ATRX promotes gene expression by facilitating transcriptional elongation through guanine-rich coding regions - Levy_2015_Hum.Mol.Genet_24_1824