TY  - GEN
AU  - Güngör,O
AU  - Kirik,S
AU  - Cevizli,D
AU  - Karaokur,F
AU  - Ozer,L
AU  - Uysal,S
AU  - Dilber,C
TI  - A RETT SYNDROME CASE WITH NOVEL NON-IDENTICAL MUTATION IN MECP2 GENE
SN  - 1015-8146
PY  - 2016///0303
KW  - Child, Preschool
KW  - Female
KW  - Humans
KW  - Methyl-CpG-Binding Protein 2
KW  - genetics
KW  - Mutation
KW  - Rett Syndrome
N1  - Publication Type: Case Reports; Journal Article
ER  -