TY  - GEN
AU  - Ishii,T
AU  - Makita,Y
AU  - Ogawa,A
AU  - Amamiya,S
AU  - Yamamoto,M
AU  - Miyamoto,A
AU  - Oki,J
TI  - The role of different X-inactivation pattern on the variable clinical phenotype with Rett syndrome
SN  - 0387-7604
PY  - 2002///0313
KW  - Adult
KW  - Allelic Imbalance
KW  - genetics
KW  - Amino Acid Sequence
KW  - Base Sequence
KW  - Chromosomal Proteins, Non-Histone
KW  - DNA Mutational Analysis
KW  - DNA-Binding Proteins
KW  - Disease Progression
KW  - Dosage Compensation, Genetic
KW  - Female
KW  - Humans
KW  - Male
KW  - Methyl-CpG-Binding Protein 2
KW  - Mutation
KW  - Pedigree
KW  - Phenotype
KW  - Point Mutation
KW  - Repressor Proteins
KW  - Rett Syndrome
KW  - Twins, Monozygotic
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1016/s0387-7604(01)00344-8
ER  -