Mihai Miclăuș & Gabriel Balmus. (2024). CRISPR-Cas9-directed gene therapy for spinocerebellar ataxia type 1. Elsevier.
Chicago Style (17th ed.) CitationMihai Miclăuș and Gabriel Balmus. CRISPR-Cas9-directed Gene Therapy for Spinocerebellar Ataxia Type 1. Elsevier, 2024.
MLA (9th ed.) CitationMihai Miclăuș and Gabriel Balmus. CRISPR-Cas9-directed Gene Therapy for Spinocerebellar Ataxia Type 1. Elsevier, 2024.
Warning: These citations may not always be 100% accurate.