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

Overview of attention for article published in Orphanet Journal of Rare Diseases, December 2019

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Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa. https://t.co/VYK8f0pijE #Neuralstemcells

21 Dec 2019

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