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Extending the clinical spectrum of SPG3A mutations to a very severe and very early complicated phenotype

✍ Scribed by J. Haberlová; K. G. Claeys; J. Zámečník; P. De Jonghe; P. Seeman


Book ID
106093824
Publisher
Springer
Year
2008
Tongue
English
Weight
296 KB
Volume
255
Category
Article
ISSN
0340-5354

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