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ÖS
Özlem Sezer
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:
10
/
i10-index:
11
Reputation
Biology
< 1%
Chemistry
< 1%
Economics
< 1%
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Overview
Publications
2
Peer Reviews
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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
Hyperekplexia: A Single-Center Experience
Merve Dolu
et al.
Jul 25, 2024
Hyperekplexia is a rare neurogenetic disorder that is classically characterized by an exaggerated startle response to sudden unexpected stimuli. This study aimed to determine clinical and genetic characteristics of our patients with hyperekplexia.
Genetics
Pulmonary And Respiratory Medicine
0
Paper
Genetics
Pulmonary And Respiratory Medicine
0
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