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Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis
- Guicheney, P (author)
- Vignier, N (author)
- HelblingLeclerc, A (author)
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- Nissinen, M (author)
- Zhang, X (author)
- Cruaud, C (author)
- Lambert, JC (author)
- Richelme, C (author)
- Topaloglu, H (author)
- Merlini, L (author)
- Barois, A (author)
- Schwartz, K (author)
- Tome, FMS (author)
- Fardeau, M (author)
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- (creator_code:org_t)
- 1997
- 1997
- English.
- In: Neuromuscular disorders : NMD. - 0960-8966. ; 7:3, s. 180-186
- Journal article (peer-reviewed)
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- Guicheney, P
- Vignier, N
- HelblingLeclerc, ...
- Nissinen, M
- Zhang, X
- Cruaud, C
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- Lambert, JC
- Richelme, C
- Topaloglu, H
- Merlini, L
- Barois, A
- Schwartz, K
- Tome, FMS
- Tryggvason, K
- Fardeau, M
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- Neuromuscular di ...
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- Karolinska Institutet
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