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About this Biochemistry, Genetics and Molecular Biology article

Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia-oculomotor apraxia 4 and pilocytic astrocytoma by Scholz, C.; Golas, M.M.; Weber, R.G.; Hartmann, C.; Lehmann, U.; Sahm, F.; Schmidt, G.; Auber, B.; Sturm, M.; Schlegelberger, B.; Illig, T.; Steinemann, D.; Hofmann, W. is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Scholz, C.; Golas, M.M.; Weber, R.G.; Hartmann, C.; Lehmann, U.; Sahm, F.; Schmidt, G.; Auber, B.; Sturm, M.; Schlegelberger, B.; Illig, T.; Steinemann, D.; Hofmann, W.
Publisher
John Wiley and Sons; Wiley (Blackwell Publishing); Blackwell Publishing Inc.; Wiley (ISSN 0009-9163)
Published
2018
Language
EN
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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Browse all works by Scholz, C.; Golas, M.M.; Weber, R.G.; Hartmann, C.; Lehmann, U.; Sahm, F.; Schmidt, G.; Auber, B.; Sturm, M.; Schlegelberger, B.; Illig, T.; Steinemann, D.; Hofmann, W.