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TMEM5
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The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan …
TMEM5-associated dystroglycanopathy presenting with CMD and mild limb-girdle muscle involvement.
The Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functio…
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly.
Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry.
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