Erratum: Identification of a recurrent mutation inGALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders (Journal of Molecular Medicine (2005) 83 (33-38) DOI: org/10.1007/s00109-004-0610-8)

Yaacov Frishberg, Orit Topaz, Reuven Bergman, Doron Behar, Drora Fisher, Derek Gordon, Gabriele Richard, Eli Sprecher*

*Corresponding author for this work

Research output: Contribution to journalComment/debate

Original languageEnglish
Pages (from-to)240
Number of pages1
JournalJournal of Molecular Medicine
Issue number3
StatePublished - Mar 2005
Externally publishedYes

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