![Multigene panel next generation sequencing in a patient with cherry red macular spot: Identification of two novel mutations in NEU1 gene causing sialidosis type I associated with mild to unspecific biochemical and Multigene panel next generation sequencing in a patient with cherry red macular spot: Identification of two novel mutations in NEU1 gene causing sialidosis type I associated with mild to unspecific biochemical and](https://ars.els-cdn.com/content/image/1-s2.0-S2214426916300738-gr1.jpg)
Multigene panel next generation sequencing in a patient with cherry red macular spot: Identification of two novel mutations in NEU1 gene causing sialidosis type I associated with mild to unspecific biochemical and
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PDF) Fundus autofluorescence and optical coherence tomography of a macular cherry-red spot in a case report of sialidosis
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