Biography and Research Information
OverviewAI-generated summary
Richard E Frye's research focuses on understanding genetic factors contributing to health conditions. His recent publication examines a complex heterozygous polymerase gamma mutation and its association with cerebral folate deficiency in a pediatric patient experiencing refractory partial status epilepticus. This work highlights the intricate relationship between specific genetic alterations and neurological disorders in children. Frye collaborates with Raghu Ramakrishnaiah at the University of Arkansas for Medical Sciences, with whom he has co-authored one publication. His scholarly output includes one total publication.
Metrics
- Publications: 1
Selected Publications
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Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status (2022)
Collaboration Network
Top Collaborators
Debopam Samanta
University of Arkansas for Medical Sciences
1 shared publication
In database
- Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status
Raghu Ramakrishnaiah
University of Arkansas for Medical Sciences
1 shared publication
In database
- Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status
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