APA (7th ed.) Citation
(2026). A Novel MYO5A Mutation (c.3508C>T) in a 27-Month-Old Girl With Hypotonia and Developmental Delay: Expanding the Phenotypic Spectrum of Griscelli Syndrome Type 1. Case Reports in Immunology.
Chicago Style (17th ed.) Citation
"A Novel MYO5A Mutation (c.3508C>T) in a 27-Month-Old Girl With Hypotonia and Developmental Delay: Expanding the Phenotypic Spectrum of Griscelli Syndrome Type 1." Case Reports in Immunology 2026.
MLA (9th ed.) Citation
"A Novel MYO5A Mutation (c.3508C>T) in a 27-Month-Old Girl With Hypotonia and Developmental Delay: Expanding the Phenotypic Spectrum of Griscelli Syndrome Type 1." Case Reports in Immunology, 2026.
Warning: These citations may not always be 100% accurate.