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Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland
Luca Trotta, Timo Hautala, Sari Hämäläinen, Jaana Syrjänen, Hanna Viskari, Henrikki Almusa, Maija Lepisto, Meri Kaustio, Kimmo Porkka, Aarno Palotie, Mikko Seppänen, Janna Saarela
Eur J Hum Genet. 2016 Oct; 24(10): 1473–1478. Published online 2016 May 4. doi: 10.1038/ejhg.2016.37
PMCID:
PMC5027683
AbstractArticlePDF–998K

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