- Sialidosis Type I without a Cherry Red Spot— Is There a Genetic Basis?
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Neeraja K, Holla VV, Prasad S, Surisetti BK, Rakesh K, Kamble N, Yadav R, Pal PK
- KMID: 2511490
- J Mov Disord.
- 2021 Jan;14(1):65-69.
- doi: 10.14802/jmd.20083
Sialidosis is an inborn error of metabolism due to a defect in the NEU1 gene and manifests as two phenotypes: mild type I and severe type II. The cherry red... -
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