Whole Exome Sequencing Reveals Uncommon Mutations in the Recently Identified Fanconi Anemia Gene SLX4/FANCP

B. Schuster, K. Knies, C. Stoepker, E. Velleuer, R. Friedl, B. Gottwald-Muhlhauser, J.P. de Winter, D. Schindler

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)93-96
JournalHuman Mutation
Volume34
Issue number1
DOIs
Publication statusPublished - 2013

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Schuster, B., Knies, K., Stoepker, C., Velleuer, E., Friedl, R., Gottwald-Muhlhauser, B., ... Schindler, D. (2013). Whole Exome Sequencing Reveals Uncommon Mutations in the Recently Identified Fanconi Anemia Gene SLX4/FANCP. Human Mutation, 34(1), 93-96. https://doi.org/10.1002/humu.22221