eP079: Cerebellar atrophy, developmental delay and a VUS in the THG1L gene: A case report

Baptiste, C., & Pereira, E. (2022). eP079: Cerebellar atrophy, developmental delay and a VUS in the THG1L gene: A case report. Genetics in Medicine, 24(3), S52. https://doi.org/10.1016/j.gim.2022.01.116
Authors:
Caitlin Baptiste
Elaine Cristina Pereira
Affiliated Authors:
Caitlin Baptiste
Elaine Cristina Pereira
Columbia Affiliation:
Subjects:
Molecular Mechanisms of Cardiac Development and Regeneration (OpenAlex Topic)
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Publication Type:
Article
Unique ID:
10.1016/j.gim.2022.01.116
DOI:
10.1016/j.gim.2022.01.116
Journal:
Genetics in Medicine
Publication Date:
Data Source:
OpenAlex
Source Link:
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