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KK
Kadri Karaer
Author with expertise in Molecular Basis of Rett Syndrome and Related Disorders
Achievements
Cited Author
Open Access Advocate
Key Stats
Upvotes received:
0
Publications:
2
(50% Open Access)
Cited by:
286
h-index:
12
/
i10-index:
13
Reputation
Biology
< 1%
Chemistry
< 1%
Economics
< 1%
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Overview
Publications
2
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Publications
0
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease
Ender Karaca
et al.
Nov 1, 2015
Genetics
Molecular Biology
0
Paper
Genetics
286
0
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0
NRXN2 Homozygous Variant Identified in a Family with Global Developmental Delay, Severe Intellectual Disability, EEG Abnormalities and Speech Delay: A new Syndrome?
Derya Karaer
et al.
Jan 2, 2025
. This study aims to characterize the clinical phenotype of a family with two siblings exhibiting neurological manifestations, utilizing whole exome sequencing (WES) to identify potential pathogenic variants within the
Genetics
Neuroscience
0
Paper
Genetics
Neuroscience
0
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