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

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dc.contributor.authorKoprulu, Mine
dc.contributor.authorShabbir, Rana Muhammad Kamran
dc.contributor.authorZaman, Qamar
dc.contributor.authorNalbant, Gokhan
dc.contributor.authorMalik, Sajid
dc.contributor.authorTolun, Aslihan
dc.date.accessioned2025-10-16T15:19:37Z
dc.date.issued2021
dc.identifier.doi10.1016/j.ejmg.2021.104181
dc.identifier.otherWOS:000635182200007
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/7375
dc.publisherELSEVIER
dc.sourceEUROPEAN JOURNAL OF MEDICAL GENETICS
dc.subjectPachygyria
dc.subjectBrain atrophy
dc.subjectSulcal atrophy
dc.subjectLumbar lordosis
dc.subjectScoliosis
dc.titleCRADD and USP44 mutations in intellectual disability, mild lissencephaly, brain atrophy, developmental delay, strabismus, behavioural problems and skeletal anomalies
dc.typeArticle

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