Whole-exome sequencing identifies germline mutation in TP53 and ATRX in a child with genomically aberrant AT/RT and her mother with anaplastic astrocytoma

Kristiina Nordfors, Joonas Haapasalo, Afyounian Ebrahim, E Afyounian, Joonas Tuominen, Matti Annala, Sergei Häyrynen, Ritva Karhu, Pauli Helén, Olli Lohi, Matti Nykter, Hannu Haapasalo, Kirsi J. Granberg

Research output: Contribution to journalArticleScientificpeer-review

3 Citations (Scopus)
Original languageEnglish
Article numbera002246
Number of pages13
JournalCold Spring Harbor Molecular Case Studies
Issue number2
Publication statusPublished - Mar 2018
Publication typeA1 Journal article-refereed

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