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Publications by Lee Cyn Ang
MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients
Frontiers in Genetics
Genetics
Molecular Medicine
Clinical Neuropathology Practice Guide 6-2013: Morphology and an Appropriate Immunohistochemical Screening Panel Aid in the Identification of Synovial Sarcoma by Neuropathologists
Clinical Neuropathology
Medicine
Forensic Medicine
Pathology
Neurology
Related publications
Rett Syndrome Without MECP2 Mutation in a Pakistani Girl
Life and Science
Rett Syndrome and MeCP2
NeuroMolecular Medicine
Molecular Neuroscience
Neurology
Molecular Medicine
Cellular
Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome
Journal of Human Genetics
Genetics
MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches
Journal of Neonatal Biology
MeCP2 Mutations in Children With and Without the Phenotype of Rett Syndrome
Neurology
Neurology
Epilepsy in 11 Patients With Typical Rett Syndrome Caused by Mecp2 Mutation: Clinical and Electroencephalographic Characteristics, Course, Therapy (Results of the Authors’ Observations)
Russkii Zhunal Detskoi Nevrologii
Child Health
Neurology
Pediatrics
Perinatology
The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders
Pediatric Neurology
Child Health
Developmental Neuroscience
Pediatrics
Perinatology
Neurology
Gross Rearrangements of the MECP2 Gene Are Found in Both Classical and Atypical Rett Syndrome Patients
Journal of Medical Genetics
Genetics
Bisphosphonates and MeCP2 Deficiency: Cellular Studies and Clinical Application in Rett Syndrome
Journal of Musculoskeletal Disorders and Treatment
