Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement.
Sadler E; Klausegger A; Muss W; Deinsberger U; Pohla-Gubo G; Laimer M; Lanschuetzer C; Bauer JW; Hintner H; Archives Of Dermatology, 2006, vol. 142, issue 12, p 1619, ISSN 0003987x. ISBN 0003987x.

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