Homozygous disruption of PDZD7 by reciprocal translocation...

Human Molecular Genetics 2009 / 02 Vol. 18; Iss. 4

Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment

Schneider, E., Marker, T., Daser, A., Frey-Mahn, G., Beyer, V., Farcas, R., Schneider-Ratzke, B., Kohlschmidt, N., Grossmann, B., Bauss, K., Napiontek, U., Keilmann, A., Bartsch, O., Zechner, U., Wolf
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Volume:
18
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddn395
Date:
February, 2009
File:
PDF, 545 KB
english, 2009
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