NARA Discovery
Article Details
← Back to Search Results
Journal Article

Identification of a recurrent mutation in GALNT3 demonstrates 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
Journal of Molecular Medicine · Vol. 83, Issue 3 · pp. 240-240 · 2005

Abstract

Abstract is unavailable.

Bibliographic Information

JournalJournal of Molecular Medicine
PublisherSpringer
Publication Date2005-03-01
Publication Year2005
Volume83
Issue3
Pages240-240
Document TypeJournal Article
Print ISSN0946-2716
eISSN1432-1440
DOI10.1007/s00109-005-0654-4

Access Information

NARA Access Coverage1922-01-01~Current
Journal Homepagehttps://www.springer.com/journal/109
Publisher PageOpen Publisher Page
Full-text access depends on NARA's subscribed coverage and institutional access.