Open AccessHydrocephalus in mouse B3glct mutants is likely caused by defects in multiple B3GLCT substrates in ependymal cells and subcommissural organ
Author(s) -
Sanjiv Neupane,
June Goto,
Steven J. Berardinelli,
Atsuko Ito,
Robert S. Haltiwanger,
Bernadette C. Holdener
Publication year - 2021
Publication title -
glycobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.757
H-Index - 128
eISSN - 1460-2423
pISSN - 0959-6658
DOI - 10.1093/glycob/cwab033
Subject(s) - subcommissural organ , ependymal cell , biology , mutant , thrombospondin , microbiology and biotechnology , endocrinology , gene , genetics , metalloproteinase , central nervous system , matrix metalloproteinase
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