Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Details
Original language | English |
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Pages (from-to) | 62-63 |
Number of pages | 2 |
Journal | European journal of pediatrics |
Volume | 165 |
Issue number | 1 |
Publication status | Published - Jan 2006 |
Peer-reviewed | Yes |
External IDs
PubMed | 16143867 |
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