Identification of a recurrent mutation inGALNT3demonstrates...

Journal of Molecular Medicine 2005 / 01 Vol. 83; Iss. 1

Identification of a recurrent mutation inGALNT3demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders

Yaacov Frishberg, Orit Topaz, Reuven Bergman, Doron Behar, Drora Fisher, Derek Gordon, Gabriele Richard, Eli Sprecher
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Volume:
83
Language:
english
Pages:
6
DOI:
10.1007/s00109-004-0610-8
Date:
January, 2005
File:
PDF, 335 KB
english, 2005
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