Spontaneous recurrent mutations and a complex rearrangement in the MECP2 gene in the light of current models of mutagenesis. [electronic resource]
- Mutation research Jun 2012
- 69-72 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0027-5107
10.1016/j.mrfmmm.2012.04.001 doi
Base Sequence Female Humans Infant Infant, Newborn Methyl-CpG-Binding Protein 2--genetics Molecular Sequence Data Mutation Rett Syndrome--genetics Translocation, Genetic