CRADD and USP44 mutations in intellectual disability, mild lissencephaly, brain atrophy, developmental delay, strabismus, behavioural problems and skeletal anomalies-Reference-Cited by-同舟云学术

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

Published:2021-04 Issue:4 Volume:64 Page:104181
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Koprulu Mine,Shabbir Rana Muhammad Kamran,Zaman Qamar,Nalbant Gökhan,Malik Sajid^ORCID,Tolun Aslıhan^ORCID

Funder

Quaid-i-Azam University

TÜBİTAK

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

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4. Mutations in CRADD result in reduced caspase-2-mediated neuronal apoptosis and cause megalencephaly with a rare lissencephaly variant;Di Donato;Am. J. Hum. Genet.,2016

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