## Abstract As caveolin‐3 deficiencies may explain persistent hyper‐CK‐emia, we performed __CAV3__ gene mutation analysis and immunohistochemistry for caveolin‐3 in 31 patients with idiopathic hyper‐CK‐emia. In 2 of 29 patients who donated blood, variants in the __CAV3__ gene were detected. Althoug
CAPN3 mutations in patients with idiopathic eosinophilic myositis
✍ Scribed by Martin Krahn; Adolfo Lopez De Munain; Nathalie Streichenberger; Rafaëlle Bernard; Christophe Pécheux; Hervé Testard; José L. Pena-Segura; Eugenia Yoldi; Ana Cabello; Norma B. Romero; Juan J. Poza; Sandrine Bouillot-Eimer; Xavier Ferrer; Maria Goicoechea; Federico Garcia-Bragado; France Leturcq; J. Andoni Urtizberea; Nicolas Lévy
- Book ID
- 102705358
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 885 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0364-5134
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