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A double point mutation in the DNA-binding region of Egr2 switches its function from inhibition to induction of proliferation: A potential contribution to the development of congenital hypomyelinating neuropathy

✍ Scribed by Peter Arthur-Farraj; Rhona Mirsky; David B. Parkinson; Kristjan R. Jessen


Book ID
113812059
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
630 KB
Volume
24
Category
Article
ISSN
0969-9961

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