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No correlation between amount of aberrant transcript and severity of phenotype in hereditary spastic paraplegia patients with a c.1242A > G splice mutation in theSPG4gene

✍ Scribed by S. M. Sauter; N. Dörwald; W. Engel; J. Neesen


Publisher
Springer
Year
2005
Tongue
English
Weight
252 KB
Volume
253
Category
Article
ISSN
0340-5354

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