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Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy

✍ Scribed by Juliane Ramser; Mary Ellen Ahearn; Claus Lenski; Kemal O. Yariz; Heide Hellebrand; Michael von Rhein; Robin D. Clark; Rita K. Schmutzler; Peter Lichtner; Eric P. Hoffman; Alfons Meindl; Lisa Baumbach-Reardon


Book ID
116195568
Publisher
American Society of Human Genetics
Year
2008
Tongue
English
Weight
612 KB
Volume
82
Category
Article
ISSN
0002-9297

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