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Schmalbruch et al., 2001 - Google Patents

Spinal muscular atrophy: present state

Schmalbruch et al., 2001

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Document ID
15795704166925157389
Author
Schmalbruch H
Haase G
Publication year
Publication venue
Brain pathology

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Snippet

Spinal muscular atrophy (SMA) is a hereditary neurodegenerative disease caused by homozygous deletions or mutations in the SMN1 gene on Chr. 5q13. SMA spans from severe Werdnig‐Hoffmann disease (SMA 1) to relatively benign Kugelberg‐Welander …
Continue reading at www.ncbi.nlm.nih.gov (PDF) (other versions)

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    • A61K38/1703Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
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    • C07K14/4712Cystic fibrosis
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