Amanote Research
Register
Sign In
Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome
Journal of Human Genetics
- United Kingdom
doi 10.1007/s100380070032
Full Text
Open PDF
Abstract
Available in
full text
Categories
Genetics
Date
July 1, 2000
Authors
K. Amano
Y. Nomura
M. Segawa
K. Yamakawa
Publisher
Springer Science and Business Media LLC
Related search
Rett Syndrome and MeCP2
NeuroMolecular Medicine
Molecular Neuroscience
Neurology
Molecular Medicine
Cellular
Gross Rearrangements of the MECP2 Gene Are Found in Both Classical and Atypical Rett Syndrome Patients
Journal of Medical Genetics
Genetics
MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches
Journal of Neonatal Biology
MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients
Frontiers in Genetics
Genetics
Molecular Medicine
MeCP2 Mutations in Children With and Without the Phenotype of Rett Syndrome
Neurology
Neurology
Rett Syndrome Without MECP2 Mutation in a Pakistani Girl
Life and Science
The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders
Pediatric Neurology
Child Health
Developmental Neuroscience
Pediatrics
Perinatology
Neurology
Mosaic MECP2 Variants in Males With Classical Rett Syndrome Features, Including Stereotypical Hand Movements
Clinical Genetics
Genetics
EEG Findings in Patients With Rett Syndrome
Journal of the Turkish Epilepsi Society