2021
DOI: 10.1016/j.ejmg.2021.104181
|View full text |Cite
|
Sign up to set email alerts
|

CRADD and USP44 mutations in intellectual disability, mild lissencephaly, brain atrophy, developmental delay, strabismus, behavioural problems and skeletal anomalies

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 8 publications
(1 citation statement)
references
References 25 publications
0
1
0
Order By: Relevance
“…Although Cradd has not been implicated in the reproductive system, it has been associated with intellectual disability (ID) and anencephaly (Koprulu et al, 2021). Cradd, together with PIDD1 (p53-induced death domain protein 1) and caspase-2, forms PIDDosome, a multiprotein complex that responds to DNA damage by inducing apoptosis (Sheikh et al, 2021).…”
Section: Discussionmentioning
confidence: 99%
“…Although Cradd has not been implicated in the reproductive system, it has been associated with intellectual disability (ID) and anencephaly (Koprulu et al, 2021). Cradd, together with PIDD1 (p53-induced death domain protein 1) and caspase-2, forms PIDDosome, a multiprotein complex that responds to DNA damage by inducing apoptosis (Sheikh et al, 2021).…”
Section: Discussionmentioning
confidence: 99%