Hussain, A., Acharya, A., Bharadwaj, T., Genomics, U. O. W. C. F. M., Leal, S. M., Khaliq, A., Mir, A., & Schrauwen, I. (2023). A Novel Variant in VPS13B Underlying Cohen Syndrome. BioMed Research International, 2023(1). Portico. https://doi.org/10.1155/2023/9993801
Subjects:
Intellectual Disability
(MeSH)
Microcephaly
(MeSH)
Genetic Basis of Neutropenia Disorders
(OpenAlex Topic)
Genetic Basis of Primary Immunodeficiency Disorders
(OpenAlex Topic)
Standards and Guidelines for Genetic Variant Interpretation
(OpenAlex Topic)
Publication Type:
Article
Unique ID:
10.1155/2023/9993801
PMID:
DOI:
Journal:
Publication Date:
Data Source:
OpenAlex
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