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A Novel 4 bp Deletion Mutation in the FALDH Gene Segregating in a Turkish Family with Sjögren–Larsson Syndrome  Michel A.A.P. Willemsen, Peter M. Steijlen,

Published byBenjamin van der Horst Modified over 5 years ago

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Presentation on theme: "A Novel 4 bp Deletion Mutation in the FALDH Gene Segregating in a Turkish Family with Sjögren–Larsson Syndrome  Michel A.A.P. Willemsen, Peter M. Steijlen,"— Presentation transcript:

1 A Novel 4 bp Deletion Mutation in the FALDH Gene Segregating in a Turkish Family with Sjögren–Larsson Syndrome  Michel A.A.P. Willemsen, Peter M. Steijlen, Jan G.N. de Jong, Jan J. Rotteveel, Lodewijk Ijlst, Michiel A. van Werkhoven, Ronald J.A. Wanders  Journal of Investigative Dermatology  Volume 112, Issue 5, Pages (May 1999) DOI: /j x Copyright © 1999 The Society for Investigative Dermatology, Inc Terms and Conditions

2 Figure 1 Electropherogram of a control subject, patient 1 (the identical pattern of patient 2 is not shown). and both parents. The sequence surrounding the 4 bp deletion (1384–1387delGAAA, indicated by an arrow) in the FALDH gene is shown. Journal of Investigative Dermatology  , DOI: ( /j x) Copyright © 1999 The Society for Investigative Dermatology, Inc Terms and Conditions

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