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ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.
- Greenway, Matthew J (author)
-
- Andersen, Peter M (author)
- Umeå universitet,Neurologi
- Russ, Carsten (author)
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- Ennis, Sean (author)
- Cashman, Susan (author)
- Donaghy, Colette (author)
- Patterson, Victor (author)
- Swingler, Robert (author)
- Kieran, Dairin (author)
- Prehn, Jochen (author)
- Morrison, Karen E (author)
- Green, Andrew (author)
- Acharya, K Ravi (author)
- Brown, Robert H (author)
- Hardiman, Orla (author)
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- (creator_code:org_t)
- 2006
- 2006
- English.
- In: Nat Genet. - 1061-4036. ; 38:4, s. 411-3
- Journal article (peer-reviewed)
Subject headings
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Keyword
- Adult
- Aged
- Aged; 80 and over
- Amyotrophic Lateral Sclerosis/*genetics
- Female
- Humans
- Male
- Middle Aged
- Models; Molecular
- Mutation; Missense
- Pedigree
- Protein Conformation
- Ribonuclease; Pancreatic/chemistry/*genetics
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- ref (subject category)
- art (subject category)
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- Russ, Carsten
- Ennis, Sean
- Cashman, Susan
- Donaghy, Colette
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- Patterson, Victo ...
- Swingler, Robert
- Kieran, Dairin
- Prehn, Jochen
- Morrison, Karen ...
- Green, Andrew
- Acharya, K Ravi
- Brown, Robert H
- Hardiman, Orla
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- Nat Genet
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- Umeå University
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