Human Molecular Genetics

Journal Abbreviation: HUM MOL GENET
ISSN: 0964-6906
eISSN: 1460-2083
Publisher: Oxford University Press (OUP): Policy B - Oxford Open Option B

Publications (54)

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Abstract

Translation of SOX10 3' untranslated region causes a complex severe neurocristopathy by generation of a deleterious functional domain. (2007) Wegner M Journal article, Original article Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia (2003) Sock E, Wegner M Journal article, Original article Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome (2000) Sock E, Wegner M Journal article, Original article A molecular analysis of the Yemenite deaf-blind hypopigmentation syndrome: Sox10 dysfunction causes different neurocristopathies (1999) Wegner M Journal article, Original article
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