Unusual type of neural muscular atrophy with a possible X-chromosomal inheritance pattern

Author:

Skre H.,Mellgren S. I.,Bergsholm P.,Slagsvold J. E.

Publisher

Wiley

Subject

Neurology (clinical),Neurology,General Medicine

Reference10 articles.

1. A clinical and genetic study of chronic proximal spinal muscular atrophy;Bundey;Brain,1975

2. Über chronische spinale Muskelatrophie im Kindesalter auf familiärer Basis;Hoffmann;Dtsch. Z. Nervenheilk.,1893

3. Familial “mitochondrial” myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibers. Part 1. Clinical, electrophysiological and pathological findings. J. Neurol;Hudgson;Sci.,1972

4. Progressive proximal spinal and bulbar muscular atrophy of late onset;Kennedy;Neurology (Minneap.),1968

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1. Amyotrophic lateral sclerosis: lessons from mouse and human genetics;Clinical Neuroscience Research;2001-01

2. Spinale Muskelatrophien;Monogen bedingte Erbkrankheiten 1;2000

3. Clinical Aspects of CAG Repeat Diseases;Brain Pathology;1997-07

4. Genetic Anticipation;Neurologic Clinics;1994-11

5. Molecular basis and diagnosis of neurogenetic disorders;Journal of the Neurological Sciences;1994-07

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