Novel RPS6KA3 mutations cause Coffin-Lowry syndrome in two patients and concurrent compulsive eyebrow-pulling behavior in one of them
Departments of aPediatric Genetics
bMedical Genetics
cPediatric Psychiatry, S.B.Ü Dr. Behçet Uz Children’s Education and Research Hospital, Izmir, Turkey
Received 28 January 2022 Accepted 7 July 2022
Correspondence to Semra Gürsoy, MD, Department of Pediatric Genetics, S.B.Ü Dr. Behçet Uz Children’s Education and Research Hospital, Sezer Doğan Street, No.11, Izmir 35210 Turkey, Tel: +905063672451; e-mail: [email protected]
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