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ArticleCase reports in immunology2026

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.

Davoud AmirKashani et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2026

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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. | OpenQuestion