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Publications by Humaira Aziz Sawal

Rett Syndrome Without MECP2 Mutation in a Pakistani Girl

Life and Science
2020English

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Rett Syndrome and MeCP2

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MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients

Frontiers in Genetics
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2018English

MeCP2 Mutations in Children With and Without the Phenotype of Rett Syndrome

Neurology
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2001English

MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches

Journal of Neonatal Biology
2016English

The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders

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Bisphosphonates and MeCP2 Deficiency: Cellular Studies and Clinical Application in Rett Syndrome

Journal of Musculoskeletal Disorders and Treatment
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Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome

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2000English

Mosaic MECP2 Variants in Males With Classical Rett Syndrome Features, Including Stereotypical Hand Movements

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2018English

A Thorough MECP2 Mutation Analysis

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2008English

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