Shingo Koyama, Hidenori Sato, Manabu Wada, Toru Kawanami, Mitsuru Emi, & Takeo Kato. (2017). Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders. BMC.
Chicago Style (17th ed.) CitationShingo Koyama, Hidenori Sato, Manabu Wada, Toru Kawanami, Mitsuru Emi, and Takeo Kato. Whole-exome Sequencing and Digital PCR Identified a Novel Compound Heterozygous Mutation in the NPHP1 Gene in a Case of Joubert Syndrome and Related Disorders. BMC, 2017.
MLA (9th ed.) CitationShingo Koyama, et al. Whole-exome Sequencing and Digital PCR Identified a Novel Compound Heterozygous Mutation in the NPHP1 Gene in a Case of Joubert Syndrome and Related Disorders. BMC, 2017.
Warning: These citations may not always be 100% accurate.