Niemann-Pick type C disease with a novel intronic mutation: three Turkish cases from the same family.
Gonca Kilic YildirimCoskun YararBerna Seker YilmazSerdar CeylanerPublished in: Journal of pediatric endocrinology & metabolism : JPEM (2021)
When combined with the filipin staining and the patients' clinical outcomes, this mutation is likely to be deleterious. Moreover, cDNA sequencing supports the pathogenicity of this novel variant.