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Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland
Authors
A Durandy
A Durandy
+41 more
A Kong
A Polvi
Aarno Palotie
AM Sulonen
AV Gulino
EM Haapaniemi
ET Lim
G Meyers
Hanna Viskari
Henrikki Almusa
Jaana Syrjänen
Janna Saarela
JU Palo
Kimmo Porkka
L Peltonen
Luca Trotta
M Cogne
M Kuraoka
M Neufeld
M Ridanpaa
Maija Lepisto
Meri Kaustio
Mikko Seppänen
N Caratao
O Cabral-Marques
O Makitie
P Quartier
P Revy
R Kumar
R Norio
R Norio
RA Kittles
S Purcell
SA Mahdaviani
Sari Hämäläinen
Timo Hautala
VT Ta
W Al-Herz
WI Lee
WJ Kent
Y Minegishi
Publication date
Publisher
'Springer Science and Business Media LLC'
Doi
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Abstract
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info:doi/10.1038%2Fejhg.2016.3...
Last time updated on 03/01/2020
