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Eiberg, H
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Eiberg, H
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Deficiency of mannan-binding lectin associated serine protease-2 due to missense...
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Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)
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Novel mutation in ATP13A2 widens the spectrum of Kufor‐Rakeb syndrome (PARK9)
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Document Type
Article in Journal/Newspaper
3
Author
Eiberg, H
Bech, S
2
Friberg, L
2
Hansen, L
2
Hjermind, LE
2
Korbo, L
2
Svenstrup, K
2
Christensen, IJ
1
Gadjeva, M
1
Ip, WK
1
Jensenius, JC
1
Lau, YL
1
Nielsen, IM
1
Nielsen, Inge-Merete
1
Nielsen, JE
1
Nielsen, Jørgen Erik
1
Olsen, OR
1
Olsen, Or
1
Pinborg, LH
1
Pinborg, Lh
1
Reason, IJM
1
Ruseva, M
1
Steffensen, R
1
Thiel, S
1
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Topic
African Continental Ancestry Group - Genetics
1
Asian Continental Ancestry Group - Genetics
1
Brazil
1
Dna
1
Dna Primers
1
Exons - Genetics
1
Gene Frequency
1
Genetic
1
Genotype
1
Greenland
1
Hong Kong
1
Humans
1
Indians
1
Inuits - Genetics
1
Mannose-Binding Protein-Associated Serine Proteases - Deficiency - Genetics
1
Missense - Genetics
1
Mutation
1
Polymorphism
1
Sequence Analysis
1
South American - Genetics
1
Zambia
1
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Content Provider
University of Copenhagen: Research
1
University of Hong Kong: HKU Scholars Hub
1
Wiley Online Library
1
Geographic location
Friberg
2
Greenland
1
Language
English
3
Open Polar Keyword
greenlandic
2
inuit
2
Greenland
1
inuits
1
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