Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy.
| Autor: | von der Hagen M; Department of Paediatric Neurology, Children's Hospital, Technical University Dresden, Fetscherstrasse 74, 01307, Dresden, Germany. Maja.v.d.Hagen@uniklinikum-dresden.de, Kaindl AM, Koehler K, Mitzscherling P, Häusler HJ, Stoltenburg-Didinger G, Huebner A |
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| Jazyk: | angličtina |
| Zdroj: | European journal of pediatrics [Eur J Pediatr] 2006 Jan; Vol. 165 (1), pp. 62-3. Date of Electronic Publication: 2005 Sep 06. |
| DOI: | 10.1007/s00431-005-1752-6 |
| Databáze: | MEDLINE |
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