Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensities [version 1; referees: 2 approved]

MLA

Mohan Narayanan, et al. “Case Report: Compound Heterozygous Nonsense Mutations in TRMT10A Are Associated with Microcephaly, Delayed Development, and Periventricular White Matter Hyperintensities [Version 1; Referees: 2 Approved].” F1000Research, vol. 4, Sept. 2015. EBSCOhost, https://doi.org/10.12688/f1000research.7106.1.

APA

Mohan Narayanan, Keri Ramsey, Theresa Grebe, Isabelle Schrauwen, Szabolcs Szelinger, Matthew Huentelman, David Craig, Vinodh Narayanan, & C4RCD Research Group. (2015). Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensities [version 1; referees: 2 approved]. F1000Research, 4. https://doi.org/10.12688/f1000research.7106.1

Chicago

Mohan Narayanan, Keri Ramsey, Theresa Grebe, Isabelle Schrauwen, Szabolcs Szelinger, Matthew Huentelman, David Craig, Vinodh Narayanan, and C4RCD Research Group. 2015. “Case Report: Compound Heterozygous Nonsense Mutations in TRMT10A Are Associated with Microcephaly, Delayed Development, and Periventricular White Matter Hyperintensities [Version 1; Referees: 2 Approved].” F1000Research 4 (September). doi:10.12688/f1000research.7106.1.