Publications by authors named "Christine van Mol"

8Publications

Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.

Nat Genet 2016 10 29;48(10):1185-92. Epub 2016 Aug 29.

Faculty of Biology, Medicine and Health, School of Biological Sciences, Division of Evolution and Genomic Sciences, University of Manchester, Manchester, UK.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045717PMC
http://dx.doi.org/10.1038/ng.3661DOI Listing
October 2016

Two novel deletions in hypotonia-cystinuria syndrome.

Mol Genet Metab 2012 Nov 26;107(3):614-6. Epub 2012 Jun 26.

Laboratory for Biochemical Neuroendocrinology, Center for Human Genetics, University of Leuven, KU Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ymgme.2012.06.011DOI Listing
November 2012

Factor II gene(prothrombin G20210A)mutation and neonatal cerebrovenous thrombosis.

Thromb Haemost 2004 Oct;92(4):719-21

Erasmus Medical Center, Sophia Children's Hospital, Dr. Molewaterplein 60, 3015 GJ Rotterdam, The Netherlands.

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October 2004