Concepedia

Publication | Open Access

Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland

DOIFull Paper Access

26

Citations

22

References

2016

Year

Luca Trotta, Timo Hautala, Sari Hämäläinen, Jaana Syrjänen, Hanna Viskari, Henrikki Almusa, Maija Lepistö, Meri Kaustio, Kimmo Porkka, Aarno Palotie,
European Journal of Human Genetics

References

YearCitations

Page 1