Compound Heterozygosity of Two MECP2 Deletions with Paternal Inheritance of a Late-Truncating Mutation in a Female with Atypical Rett Syndrome (P4.253)

April 22, 2015April 6, 2015Free AccessCompound heterozygosity of two MECP2 deletions with paternal inheritance of a late-truncating mutation in a female with atypical Rett syndrome (P4.253)Amanda Lindy, Melissa Rumple, Melanie Morrow, Anita Shanmugham, Tamara Zach, and Dianalee McKnightAuthors Info & AffiliationsApril 6, 2015 issue84 (14_supplement)https://doi.org/10.1212/WNL.84.14_supplement.P4.253 Letters to the Editor