about
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt SignalingDe novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder.CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageAuthor Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageAuthor Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
P50
description
researcher, ORCID id # 0000-0002-9825-3625
@en
wetenschapper
@nl
name
Lot Snijders Blok
@ast
Lot Snijders Blok
@en
Lot Snijders Blok
@es
Lot Snijders Blok
@nl
type
label
Lot Snijders Blok
@ast
Lot Snijders Blok
@en
Lot Snijders Blok
@es
Lot Snijders Blok
@nl
prefLabel
Lot Snijders Blok
@ast
Lot Snijders Blok
@en
Lot Snijders Blok
@es
Lot Snijders Blok
@nl
P106
P31
P496
0000-0002-9825-3625