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

doi:10.1007/s00109-005-0654-4

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 journal › Comment/debate

Original language	English
Pages (from-to)	240
Number of pages	1
Journal	Journal of Molecular Medicine
Volume	83
Issue number	3
DOIs	https://doi.org/10.1007/s00109-005-0654-4
State	Published - Mar 2005
Externally published	Yes

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Frishberg, Y., Topaz, O., Bergman, R., Behar, D., Fisher, D., Gordon, D., Richard, G., & Sprecher, E. (2005). 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). Journal of Molecular Medicine, 83(3), 240. https://doi.org/10.1007/s00109-005-0654-4

Frishberg, Yaacov ; Topaz, Orit ; Bergman, Reuven et al. / 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). In: Journal of Molecular Medicine. 2005 ; Vol. 83, No. 3. pp. 240.

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title = "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)",

author = "Yaacov Frishberg and Orit Topaz and Reuven Bergman and Doron Behar and Drora Fisher and Derek Gordon and Gabriele Richard and Eli Sprecher",

year = "2005",

month = mar,

doi = "10.1007/s00109-005-0654-4",

language = "אנגלית",

volume = "83",

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journal = "Journal of Molecular Medicine",

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Frishberg, Y, Topaz, O, Bergman, R, Behar, D, Fisher, D, Gordon, D, Richard, G & Sprecher, E 2005, '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)', Journal of Molecular Medicine, vol. 83, no. 3, pp. 240. https://doi.org/10.1007/s00109-005-0654-4

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). / Frishberg, Yaacov; Topaz, Orit; Bergman, Reuven et al.
In: Journal of Molecular Medicine, Vol. 83, No. 3, 03.2005, p. 240.

Research output: Contribution to journal › Comment/debate

TY - JOUR

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AU - Frishberg, Yaacov

AU - Topaz, Orit

AU - Bergman, Reuven

AU - Behar, Doron

AU - Fisher, Drora

AU - Gordon, Derek

AU - Richard, Gabriele

AU - Sprecher, Eli

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SN - 0946-2716

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Frishberg Y, Topaz O, Bergman R, Behar D, Fisher D, Gordon D et al. 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). Journal of Molecular Medicine. 2005 Mar;83(3):240. doi: 10.1007/s00109-005-0654-4

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)

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