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Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family

โœ Scribed by Dai, J.; Kim, O.-H.; Cho, T.-J.; Schmidt-Rimpler, M.; Tonoki, H.; Takikawa, K.; Haga, N.; Miyoshi, K.; Kitoh, H.; Yoo, W.-J.; Choi, I.-H.; Song, H.-R.; Jin, D.-K.; Kim, H.-T.; Kamasaki, H.; Bianchi, P.; Grigelioniene, G.; Nampoothiri, S.; Minagawa, M.; Miyagawa, S.-i.; Fukao, T.; Marcelis, C.; Jansweijer, M. C. E.; Hennekam, R. C. M.; Bedeschi, F.; Mustonen, A.; Jiang, Q.; Ohashi, H.; Furuichi, T.; Unger, S.; Zabel, B.; Lausch, E.; Superti-Furga, A.; Nishimura, G.; Ikegawa, S.

Book ID
125475130
Publisher
BMJ Publishing Group
Year
2010
Tongue
English
Weight
315 KB
Volume
47
Category
Article
ISSN
0022-2593

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