ATYPICAL PRESENTATION OF Xp21 DISEASE: DYSTROPHIN ANALYSIS IN PATIENTS WITH MYALGIA OR IDIOPATHIC HYPER-CK-EMIA
- 2 Anni 1992/1994
- 41.317€ Totale Fondi
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Pubblicazioni Scientifiche
- BRAIN
CLINICAL VARIABILITY IN BECKER MUSCULAR-DYSTROPHY - GENETIC, BIOCHEMICAL AND IMMUNOHISTOCHEMICAL CORRELATES
- HUMAN MUTATION
A NOVEL NONSENSE MUTATION IN THE HUMAN DYSTROPHIN GENE
- NEUROMUSCULAR DISORDERS
A POSSIBLE MISSENSE MUTATION DETECTED IN THE DYSTROPHIN GENE BY DOUBLE-STRAND CONFORMATION ANALYSIS (DSCA)
- NEUROMUSCULAR DISORDERS
DUPLICATION OF DYSTROPHIN GENE AND DISSIMILAR CLINICAL PHENOTYPE IN THE SAME FAMILY
- NEUROREPORT
LOCALIZATION OF VINCULIN AND TALIN AT PERINEURIAL CELLS OF HUMAN SURAL NERVE
