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Volumn 49, Issue 15 Suppl, 2004, Pages 2451-2456
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Defective O-mannosyl glycosylation causes congenital muscular dystrophies
a
a
NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
DYSTROGLYCAN;
MANNOSE;
MANNOSYLTRANSFERASE;
N ACETYLGLUCOSAMINYLTRANSFERASE;
PROTEIN O MANNOSE BETA 1,2 N ACETYLGLUCOSAMINYLTRANSFERASE;
PROTEIN O MANNOSYLTRANSFERASE;
PROTEIN O-MANNOSE BETA-1,2-N-ACETYLGLUCOSAMINYLTRANSFERASE;
PROTEIN O-MANNOSYLTRANSFERASE;
ANIMAL;
BIOSYNTHESIS;
BRAIN;
CONGENITAL MALFORMATION;
EYE MALFORMATION;
GENETICS;
GLYCOSYLATION;
HUMAN;
MULTIPLE MALFORMATION SYNDROME;
MUSCULAR DYSTROPHY;
MUTATION;
PHYSIOLOGY;
REVIEW;
SYNDROME;
ABNORMALITIES, MULTIPLE;
ANIMALS;
BRAIN;
DYSTROGLYCANS;
EYE ABNORMALITIES;
GLYCOSYLATION;
HUMANS;
MANNOSE;
MANNOSYLTRANSFERASES;
MUSCULAR DYSTROPHIES;
MUTATION;
N-ACETYLGLUCOSAMINYLTRANSFERASES;
SYNDROME;
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EID: 16644403714
PISSN: 00399450
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (1)
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References (26)
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