Ren, S., Ren, S., Ren, S., Wang, Y., Tong, X., Wu, X., . . . Kong, Q. Case Report: Phenotypic heterogeneity within an NF1 family: assessment of the pathogenicity of a de novo c.6640dupA shift mutation and a splice variant with an epilepsy phenotype. Frontiers Media S.A.
Chicago Style (17th ed.) CitationRen, Sijing, et al. Case Report: Phenotypic Heterogeneity Within an NF1 Family: Assessment of the Pathogenicity of a De Novo C.6640dupA Shift Mutation and a Splice Variant with an Epilepsy Phenotype. Frontiers Media S.A.
MLA (9th ed.) CitationRen, Sijing, et al. Case Report: Phenotypic Heterogeneity Within an NF1 Family: Assessment of the Pathogenicity of a De Novo C.6640dupA Shift Mutation and a Splice Variant with an Epilepsy Phenotype. Frontiers Media S.A.
Warning: These citations may not always be 100% accurate.