Novel and recurrent ALDH3A2 mutations in Italian patients with Sjogren-Larsson syndrome
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概要
- 論文の詳細を見る
- Springer Japanの論文
- 2007-10-01
著者
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Didona Biagio
I Dermatology Division Idi-irccs
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Paradisi Mauro
Vii Dermatology Division
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Melino Gerry
Department Of Experimental Medicine Idi-irccs Biochemistry Laboratory C/o University Of Tor Vergata
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Bertini Enrico
Department Of Laboratory Medicine Unit Of Molecular Medicine Bambino Gesu Hospital
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CODISPOTI Andrea
Department of Experimental Medicine, IDI-IRCCS Biochemistry Laboratory, c/o University of Tor Vergat
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RIZZO Wiliam
University of Nebraska Medical Center
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CARNEY Gael
University of Nebraska Medical Center
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ZAMBRUNO Giovanna
Molecular Biology Laboratory
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DIONISI-VICI Carlo
Department of Laboratory Medicine, Unit of Molecular Medicine, Bambino Gesu Hospital
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PEDICELLI Cristina
VII Dermatology Division
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TERRINONI Alessandro
Department of Experimental Medicine, IDI-IRCCS Biochemistry Laboratory, c/o University of Tor Vergat
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Terrinoni Alessandro
Department Of Experimental Medicine Idi-irccs Biochemistry Laboratory C/o University Of Tor Vergata
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Codispoti Andrea
Department Of Experimental Medicine Idi-irccs Biochemistry Laboratory C/o University Of Tor Vergata
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Dionisi-vici Carlo
Department Of Laboratory Medicine Unit Of Molecular Medicine Bambino Gesu Hospital
関連論文
- Complete maternal isodisomy causing reduction to homozygosity for a novel LAMB3 mutation in Herlitz junctional epidermolysis bullosa
- Novel and recurrent ALDH3A2 mutations in Italian patients with Sjogren-Larsson syndrome