NovelTMC1 structural and splice variants associated with congenital nonsyndromic deafness in a Sudanese pedigree

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Bibliographic Details
Published in:Human mutation 2005-01, Vol.25 (1), p.100-100
Main Authors: Meyer, Christian G., Gasmelseed, Nagla M., Mergani, Adil, Magzoub, Mubarak M.A., Muntau, Birgit, Thye, Thorsten, Horstmann, Rolf D.
Format: Article
Language:English
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ISSN:1059-7794
1098-1004
DOI:10.1002/humu.9302