Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia.
Kim SJ; Bieganski T; Sohn YB; Kozlowski K; Semënov M; Okamoto N; Kim CH; Ko AR; Ahn GH; Choi YL; Park SW; Ki CS; Kim OH; Nishimura G; Unger S; Superti-Furga A; Jin DK; Human Genetics, 2011, vol. 129, issue 5, p 497, ISSN 14321203. ISBN 14321203.

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