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- HELBLINGLECLERC, A (author)
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy
- Article/chapterEnglish1995
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- 1995
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:113292335
- http://kipublications.ki.se/Default.aspx?queryparsed=id:113292335URI
- https://doi.org/10.1038/ng1095-216DOI
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- Language:English
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- ZHANG, X (author)
- TOPALOGLU, H (author)
- CRUAUD, C (author)
- TESSON, F (author)
- WEISSENBACH, J (author)
- TOME, FMS (author)
- SCHWARTZ, K (author)
- FARDEAU, M (author)
- TRYGGVASON, KKarolinska Institutet (author)
- GUICHENEY, P (author)
- Karolinska Institutet (creator_code:org_t)
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- In:Nature genetics11:2, s. 216-2181061-4036
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