WFRF:(Neri L)
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X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene
- Renieri, A (author)
- Bruttini, M (author)
- Galli, L (author)
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- Zanelli, P (author)
- Neri, T (author)
- Rossetti, S (author)
- Turco, A (author)
- Heiskari, N (author)
- Zhou, J (author)
- Gusmano, R (author)
- Massella, L (author)
- Banfi, G (author)
- Scolari, F (author)
- Sessa, A (author)
- Rizzoni, G (author)
- Pignatti, PF (author)
- Savi, M (author)
- Ballabio, A (author)
- DeMarchi, M (author)
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- (creator_code:org_t)
- 1996
- 1996
- English.
- In: American journal of human genetics. - 0002-9297. ; 58:6, s. 1192-1204
- Journal article (peer-reviewed)
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- art (subject category)
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- Renieri, A
- Bruttini, M
- Galli, L
- Zanelli, P
- Neri, T
- Rossetti, S
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- Turco, A
- Heiskari, N
- Zhou, J
- Gusmano, R
- Massella, L
- Banfi, G
- Scolari, F
- Sessa, A
- Rizzoni, G
- Tryggvason, K
- Pignatti, PF
- Savi, M
- Ballabio, A
- DeMarchi, M
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- Karolinska Institutet
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