Mutations in ATP1A3 cause alternating hemiplegia of childhood
10.1111/cge.12031
Saved in:
Main Author: | Aminkeng, F |
---|---|
Other Authors: | MEDICINE |
Format: | Editorial |
Language: | English |
Published: |
WILEY
2022
|
Subjects: | |
Online Access: | https://scholarbank.nus.edu.sg/handle/10635/235311 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
Language: | English |
Similar Items
-
PDGFRB mutation causes autosomal-dominant Penttinen syndrome
by: Aminkeng, F
Published: (2022) -
WDR45 mutations define a novel disease entity - Static Encephalopathy of Childhood with Neurodegeneration in Adulthood
by: Aminkeng, F
Published: (2022) -
DLL4 loss-of-function heterozygous mutations cause Adams-Oliver syndrome
by: Aminkeng, F
Published: (2022) -
GFI1B mutation causes autosomal dominant gray platelet syndrome
by: Aminkeng, F
Published: (2022) -
EIF2AK4 genetic mutations cause a recessive form of rare and deadly lung disease, pulmonary veno-occlusive disease
by: Aminkeng, F
Published: (2022)