Yu, H., Zou, J., Chen, X., Chen, Y., Ruan, D., Chen, Q., . . . Jiang, X. Diagnostic journey and genetic analysis of a novel homozygous CYP2U1 mutation causing autosomal recessive spastic paraplegia type 56 (SPG56) in a consanguineous family. BMC.
Chicago Style (17th ed.) CitationYu, Hong-ping, et al. Diagnostic Journey and Genetic Analysis of a Novel Homozygous CYP2U1 Mutation Causing Autosomal Recessive Spastic Paraplegia Type 56 (SPG56) in a Consanguineous Family. BMC.
MLA (9th ed.) CitationYu, Hong-ping, et al. Diagnostic Journey and Genetic Analysis of a Novel Homozygous CYP2U1 Mutation Causing Autosomal Recessive Spastic Paraplegia Type 56 (SPG56) in a Consanguineous Family. BMC.
Warning: These citations may not always be 100% accurate.