Associated Papers
Suppressor mutations in Mecp2-null mice implicate the DNA damage response in Rett syndrome pathology.
Enikanolaiye A et al.
Genome Research, 2020
32317254 (PubMed )
Supplement: supp_gr.258400.119_Supplemental_Table_S1_.xlsx › 591
Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort.
Zhang Q et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
30405208 (PubMed )
Supplement: 41436_2018_348_MOESM3_ESM.xlsx › Sheet1
Evaluation of QTc in Rett syndrome: Correlation with age, severity, and genotype.
Crosson J et al.
American Journal of Medical Genetics. Part A, 2017
Bone mass in Rett syndrome: association with clinical parameters and MECP2 mutations.
Shapiro JR et al.
Pediatric Research, 2010
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