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Publications by Michael S. Hildebrand
Does Variation in NIPA2 Contribute to Genetic Generalized Epilepsy?
Human Genetics
Genetics
Bi-Allelic Mutations in STXBP2 Reveal a Complementary Role for STXBP1 in Cytotoxic Lymphocyte Killing
Frontiers in Immunology
Allergy
Immunology
Prediction of Cochlear Implant Performance by Genetic Mutation: The Spiral Ganglion Hypothesis
Hearing Research
Sensory Systems
Somatic GNAQ Mutation in the Forme Fruste of Sturge-Weber Syndrome
Neurology: Genetics
Neurology
Genetics
Development of a Rapid Functional Assay That Predicts GLUT1 Disease Severity
Neurology: Genetics
Neurology
Genetics
Mutations in the First MyTH4 Domain ofMYO15Aare a Common Cause of DFNB3 Hearing Loss
Laryngoscope
Otorhinolaryngology
A Novel Splice Site Mutation in theRDXgene Causes DFNB24 Hearing Loss in an Iranian Family
American Journal of Medical Genetics, Part A
Genetics