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Fig. 4 | Orphanet Journal of Rare Diseases

Fig. 4

From: Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa

Fig. 4

Rod Cone Dysfunction in Full Field Electroretinogram Findings of Patient 5. Full-field electroretinogram findings of the right eye of P5 across two visits separated by 2 years demonstrated a slow decrease in both scotopic rod-specific and photopic 30 Hz flicker suggestive of slow disease progression. Normal values were demonstrated through an age-matched control patient

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