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1 Ergebnisse
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Typical Rett Syndrome in a young boy with hemizygous c.316C..:
Kaya, Ilyas
;
Coskun, Murat
;
Gulle, Zeynep Nur
...
Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı. , 2020
Link:
https://hdl.handle.net/11454/67376
RT Journal T1 <Title>Typical Rett Syndrome in a young boy with hemizygous c.316C>T mutation in MECP2 gene</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftunivege:oai:gcris.ege.edu.tr:11454_67376&Exemplar=1&LAN=DE A1 Kaya, Ilyas A1 Coskun, Murat A1 Gulle, Zeynep Nur A1 Erbilgin, Seda A1 Akalin, Ibrahim A1 Berdeli, Afig YR 2020 K1 0-Belirlenecek JF Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı LK http://dx.doi.org/https://hdl.handle.net/11454/67376 DO https://hdl.handle.net/11454/67376 SF ELIB - SuUB Bremen
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