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Poh Hui Chia
Poh Hui Chia
Item
http://www.wikidata.org/entity/Q88761366
Q88761366
about
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P50
Q54963859-40B1FCD3-B4D9-489C-B33B-1912BC716C6B
P50
Poh Hui Chia
Item
http://www.wikidata.org/entity/Q88761366
description
researcher
@en
name
Poh Hui Chia
@en
type
Item
label
Poh Hui Chia
@en
prefLabel
Poh Hui Chia
@en
P31
Q88761366-761AD3C5-7FF7-4ED0-9766-8A904FB41070
P496
Q88761366-A20B9A82-A841-47D9-B666-29BB96FBFB71
P496
0000-0001-8070-112X
P31
Afgan
P496
0000-0001-8070-112X
http://www.w3.org/2001/XMLSchema#string