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Title
Organism
2.4.2.61
Cell endogenous activities of fukutin and FKRP coexist with the ribitol xylosyltransferase, TMEM5
Homo sapiens
2.4.2.61
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly
Homo sapiens
2.4.2.61
The muscular dystrophy gene TMEM5 encodes a ribitol beta1,4-xlosyltransferase required for the functional glycosylation of dystroglycan
Homo sapiens
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