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Author
Laflamme N
Laflamme N
References (1)
1. ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies - Lemire_2021_Am.J.Hum.Genet__
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 :
View Abstract
PubMedSearch :
Lemire_2021_Am.J.Hum.Genet__
PubMedID
:
34587489
Gene_locus related to this paper:
human-ABHD16A