Nadine Kraemer

Years Active: 2017-2019
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Tao Chen, Bin Zhang, Thomas Ziegenhals, Archana B Prusty, Sebastian Fröhler, Clemens Grimm, Yuhui Hu, Bernhard Schaefke, Liang Fang, Min Zhang, Nadine Kraemer, Angela M Kaindl, Utz Fischer, Wei Chen
A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing. PLoS genetics 15 (10) (2019)
Ethiraj Ravindran, Hao Hu, Scott A Yuzwa, Luis R Hernandez-Miranda, Nadine Kraemer, Olaf Ninnemann, Luciana Musante, Eugen Boltshauser, Detlev Schindler, Angela Hübner, Hans-Christian Reinecker, Hans-Hilger Ropers, Carmen Birchmeier, Freda D Miller, Thomas F Wienker, Christoph Hübner, Angela M Kaindl
Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation. PLoS genetics 13 (4) (2017)

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