A spectrum of spinal muscular atrophy models
β Scribed by Abi Witherden
- Book ID
- 114381822
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 25 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1357-4310
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## Abstract Proximal spinal muscular atrophy, the most frequent genetic cause of childhood lethality, is caused by homozygous loss or mutation of the __SMN1__ gene on human chromosome 5, which codes for the survival motor neuron (SMN) protein. SMN plays a role in the assembly of small nuclear ribon
Articles In The Fields Of Biochemistry And Physiology, Cell Biology, Developmental Biology, Ecology, Evolution, Genetics, Immunology, Molecular Biology, Neuroscience, Microbiology And Virology, Plant Science, Structural Biology, Science And Society. Includes Index.