A RETT SYNDROME CASE WITH NOVEL NON-IDENTICAL MUTATION IN MECP2 GENE.

Güngör, O

A RETT SYNDROME CASE WITH NOVEL NON-IDENTICAL MUTATION IN MECP2 GENE. [electronic resource] - Genetic counseling (Geneva, Switzerland) 2015 - 387-92 p. digital

Publication Type: Case Reports; Journal Article

1015-8146


Child, Preschool
Female
Humans
Methyl-CpG-Binding Protein 2--genetics
Mutation--genetics
Rett Syndrome--genetics