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Publications by Mert Karakaya
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome
American Journal of Human Genetics
Genetics
Biallelic Mutations in ADPRHL2 , Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome
American Journal of Human Genetics
Genetics
Late Diagnosis of a Truncating WISP3 Mutation Results in a Severe Phenotype of Progressive Pseudorheumatoid Dysplasia.
Cold Spring Harbor molecular case studies
Biochemistry
Molecular Medicine
Genetics
Design of Job Assignment and Routing Policies in Service Logistics
Pamukkale University Journal of Engineering Sciences
Occipital Cortex Dysgenesis With White Matter Changes Due to Mutations in Laminin A2
Turkish Journal of Pediatrics
Child Health
Pediatrics
Perinatology
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