A de novo mutation affecting human TrkB associated with severe obesity and developmental delay-Reference-Cited by-同舟云学术

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A de novo mutation affecting human TrkB associated with severe obesity and developmental delay

Published:2004-10-24 Issue:11 Volume:7 Page:1187-1189
ISSN:1097-6256
Container-title:Nature Neuroscience
language:en
Short-container-title:Nat Neurosci

Author:

Yeo Giles S H,Connie Hung Chiao-Chien,Rochford Justin,Keogh Julia,Gray Juliette,Sivaramakrishnan Shoba,O'Rahilly Stephen,Farooqi I Sadaf

Publisher

Springer Science and Business Media LLC

Subject

General Neuroscience

Link

http://www.nature.com/articles/nn1336.pdf

Reference15 articles.

1. Kernie, S.G., Liebl, D.J. & Parada, L.F. EMBO J. 19, 1290–1300 (2000).

2. Xu, B. et al. Nat. Neurosci. 6, 736–742 (2003).

3. Rios, M. et al. Mol. Endocrinol. 15, 1748–1757 (2001).

4. Huang, E.J. & Reichardt, L.F. Annu. Rev. Neurosci. 24, 677–736 (2001).

5. O'Rahilly, S., Farooqi, I.S., Yeo, G.S. & Challis, B.G. Endocrinology 144, 3757–3764 (2003).

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