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Publications by Teresa M. Lee

Intragenic Deletion as a Novel Type of Mutation in Wolman Disease

Molecular Genetics and Metabolism

Molecular Biology

English

Biventricular Impella Use in Pediatric Patients With Severe Graft Dysfunction From Acute Rejection After Heart Transplantation

Artificial Organs

Biomedical Engineering

English

Related publications

Intragenic Suppression of a Deletion Mutation of the Nonstructural Gene of an Influenza a Virus.

Journal of Virology

English

A Novel p.Val244Leu Mutation in MFN2 Leads to Charcot-Marie-Tooth Disease Type 2

Italian Journal of Pediatrics

English

Homozygous Intragenic Deletion of Type I Hexokinase Gene Causes Lethal Hemolytic Anemia of the Affected Fetus

English

A Novel Mutation of the Myelin P0 Gene Segregating Charcot-Marie-Tooth Disease Type 1B Manifesting as Trigeminal Nerve Thickening

Journal of Neurology, Neurosurgery and Psychiatry

English

Identification and Characterization of a Novel 43-Bp Deletion Mutation of the ATP7B Gene in a Chinese Patient With Wilson’s Disease: A Case Report

BMC Medical Genetics

English

A Novel Deletion Mutation in KMT2A Identified in a Child With ID/DD and Blood Eosinophilia

BMC Medical Genetics

English

Intragenic Deletions in ATP7B as an Unusual Molecular Genetics Mechanism of Wilson’s Disease Pathogenesis

Multidisciplinary

English

Characterization of a Spontaneous Novel Mutation in the NPC2 Gene in a Cat Affected by Niemann Pick Type C Disease

Multidisciplinary

English

Identification and Functional Analysis of a Novel Von Willebrand Factor Mutation in a Family With Type 2A Von Willebrand Disease

Multidisciplinary

English