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Retinitis Pigmentosa

1. Abetalipoproteinemia

2. Congenital disorder of glycosylation

3. Ceroid lipofuscinosis

4. Hunter disease

5. Kearns-Sayre Syndrome

6. LCHAD deficiency

7. Mevalonic aciduria

8. NARP

9. Peroxisomal biosynthesis disorders

10. Primary retinitis pigmentosa

11. Refsum disease

12. Sjogren-Larsson syndrome (fatty alcohol oxidoreductase deficiency)

 

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