British Academy of Childhood Disability and British Paediatric Neurology Association 2020
DOI: 10.1136/archdischild-2020-rcpch.20
|View full text |Cite
|
Sign up to set email alerts
|

P07 Onasemnogene abeparvovec gene-replacement therapy (GRT) for spinal muscular atrophy (SMA): from bench to bedside

Abstract: was 1 per 614. One third of these children develops DRE and half have GDD. Aetiology can be identified in 54%. Identification of aetiology is associated with DRE and GDD.

Help me understand this report

This publication either has no citations yet, or we are still processing them

Set email alert for when this publication receives citations?

See others like this or search for similar articles