Limb-girdle muscular dystrophy 2K, protein-O-mannosyltransferase 1 transferase (Q86061): Difference between revisions
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A distrofia muscular cintura-membro tipo 2K (LGMD2K) é uma doença do músculo esquelético caracterizada pelo aparecimento de perda muscular na infância, associada a déficit intelectual. | |||
| description / en | description / en | ||
Limb-girdle muscular dystrophy type 2K (LGMD2K) is a skeletal muscle disease characterised by the onset of muscle wasting during childhood, associated with intellectual deficit. | |||
Revision as of 11:25, 15 August 2026
Limb-girdle muscular dystrophy type 2K (LGMD2K) is a skeletal muscle disease characterised by the onset of muscle wasting during childhood, associated with intellectual deficit.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_251421896 |
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| English | Limb-girdle muscular dystrophy 2K, protein-O-mannosyltransferase 1 transferase |
Limb-girdle muscular dystrophy type 2K (LGMD2K) is a skeletal muscle disease characterised by the onset of muscle wasting during childhood, associated with intellectual deficit. |
