Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Juan José Poza
Actininopathy – A New Muscular Dystrophy Caused by ACTN2 Dominant Mutations
Annals of Neurology
Neurology
Clinical and Myopathological Evaluation of Early- And Late-Onset Subtypes of Myofibrillar Myopathy
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Related publications
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
New POMT2 Mutations Causing Congenital Muscular Dystrophy: Identification of a Founder Mutation
Neurology
Neurology
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1A
Functional Defects of a Muscle-Specific Calpain, P94, Caused by Mutations Associated With Limb-Girdle Muscular Dystrophy Type 2A
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Phenotypic Behavior of Caveolin-3 Mutations That Cause Autosomal Dominant Limb Girdle Muscular Dystrophy (LGMD-1C)
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Pathology of Frontotemporal Dementia With Limb Girdle Muscular Dystrophy Caused by a DNAJB6 Mutation
Clinical Neurology and Neurosurgery
Medicine
Surgery
Neurology
Limb-Girdle Muscular Dystrophy Due to Emerin Gene Mutations
Archives of Neurology
Clinical Course of Cone Dystrophy Caused by Mutations in the RPGR Gene
Graefe's Archive for Clinical and Experimental Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy
American Journal of Human Genetics
Genetics
