Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy von Wielgosz, Matthew M, Kim, Yoon-Sang, Carney, Gael G, Zhan, Jun, Reddivari, Muralidhar, Coop, Terry, Heath, Richard J, Brown, Scott A, Nienhuis, Arthur W

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The Molecular Basis of Sjögren-Larsson Syndrome: Mutation Analysis of the Fatty Aldehyde Dehydrogenase Gene von Rizzo, William B., Carney, Gael, Lin, Zhili

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Large contiguous gene deletions in Sjögren–Larsson syndrome von Engelstad, Holly, Carney, Gael, S'Aulis, Dana, Rise, Janae, Sanger, Warren G., Rudd, M. Katharine, Richard, Gabriele, Carr, Christopher W., Abdul-Rahman, Omar A., Rizzo, William B.

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Genomic Organization, Expression, and Alternate Splicing of the Mouse Fatty Aldehyde Dehydrogenase Gene von Lin, Zhili, Carney, Gael, Rizzo, William B.

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Fatty aldehyde dehydrogenase: genomic structure, expression and mutation analysis in Sjögren–Larsson syndrome von Rizzo, William B, Lin, Zhili, Carney, Gael

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Sjögren-Larsson Syndrome Is Caused by a Common Mutation in Northern European and Swedish Patients von De Laurenzi, Vincenzo, Rogers, Geraldine R., Tarcsa, Edit, Carney, Gael, Marekov, Lyuben, Bale, Sherri J., Compton, John G., Markova, Nelli, Steinert, Peter M., Rizzo, William B.

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A Common Deletion Mutation in European Patients with Sjögren-Larsson Syndrome von Rizzo, William B., Carney, Gael, De Laurenzi, Vincenzo

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