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Typical Rett syndrome in a young boy with hemizygous c.316CT mutation in MECP2 gene
Typical Rett syndrome in a young boy with hemizygous c.316CT mutation in MECP2 gene
2019
Murat Coskun
Seda Erbilgin
Ibrahim Akalin
İlyas Kaya
Zeynep Nur Gülle
Afig Berdeli
Keywords:
Genetics
MECP2 gene
Mutation
Rett syndrome
Medicine
Biology
Correction
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