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Publications by Michael S. Hildebrand

Does Variation in NIPA2 Contribute to Genetic Generalized Epilepsy?

English

Bi-Allelic Mutations in STXBP2 Reveal a Complementary Role for STXBP1 in Cytotoxic Lymphocyte Killing

Frontiers in Immunology

English

Prediction of Cochlear Implant Performance by Genetic Mutation: The Spiral Ganglion Hypothesis

Hearing Research

Sensory Systems

English

Somatic GNAQ Mutation in the Forme Fruste of Sturge-Weber Syndrome

Neurology: Genetics

English

Development of a Rapid Functional Assay That Predicts GLUT1 Disease Severity

Neurology: Genetics

English

Mutations in the First MyTH4 Domain ofMYO15Aare a Common Cause of DFNB3 Hearing Loss

Otorhinolaryngology

English

A Novel Splice Site Mutation in theRDXgene Causes DFNB24 Hearing Loss in an Iranian Family

American Journal of Medical Genetics, Part A

English