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About this Neuroscience article

Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence by Lukacs, Marshall; Gilley, Jonathan; Zhu, Yi; Orsomando, Giuseppe; Angeletti, Carlo; Liu, Jiaqi; Yang, Xiuna; Park, Joun; Hopkin, Robert J.; Coleman, Michael P.; Zhai, R. Grace; Stottmann, Rolf W. is a Neuroscience article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Neuroscience.

Author
Lukacs, Marshall; Gilley, Jonathan; Zhu, Yi; Orsomando, Giuseppe; Angeletti, Carlo; Liu, Jiaqi; Yang, Xiuna; Park, Joun; Hopkin, Robert J.; Coleman, Michael P.; Zhai, R. Grace; Stottmann, Rolf W.
Publisher
Elsevier Science; Elsevier ; Elsevier Inc.; Elsevier BV (ISSN 0014-4886)
Published
2019
Language
EN
Field
Neuroscience (Life Sciences)

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Browse all works by Lukacs, Marshall; Gilley, Jonathan; Zhu, Yi; Orsomando, Giuseppe; Angeletti, Carlo; Liu, Jiaqi; Yang, Xiuna; Park, Joun; Hopkin, Robert J.; Coleman, Michael P.; Zhai, R. Grace; Stottmann, Rolf W.