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ttll5 protein, human
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Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series.
Impaired glutamylation of RPGRORF15 underlies the cone-dominated phenotype associated with truncatin…
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy.
PRAME expression in melanocytic proliferations with intermediate histopathologic or spitzoid feature…
Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophy.
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