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Publications by Ferruccio Galbiati

Phenotypic Behavior of Caveolin-3 Mutations That Cause Autosomal Dominant Limb Girdle Muscular Dystrophy (LGMD-1C)

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
1999English

Palmitoylation of Caveolin-1 at a Single Site (Cys-156) Controls Its Coupling to the C-SRC Tyrosine Kinase

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2001English

Related publications

Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1A

2020English

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2U

2020English

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2I

2020English

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2S

2020English

Limb-Girdle Muscular Dystrophy

2020English

Identification of Lamin a/C ( LMNA ) Gene Mutations in Korean Patients With Autosomal Dominant Emery-Dreifuss Muscular Dystrophy and Limb-Girdle Muscular Dystrophy 1B

Journal of Human Genetics
Genetics
2002English

Limb Girdle Muscular Dystrophy

2008English

Limb-Girdle Muscular Dystrophy Due to Emerin Gene Mutations

Archives of Neurology
2007English

A New Form of Autosomal Dominant Limb-Girdle Muscular Dystrophy (LGMD1G) With Progressive Fingers and Toes Flexion Limitation Maps to Chromosome 4p21

European Journal of Human Genetics
Genetics
2004English

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