Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's Syndrome
Yazar
Plaster, N
Deymeer, F
George, A
Hahn, A
Nitu, A
Serdaroglu, P
Subramony, SH
Wolfe, G
Fu, YH
Ptacek, LJ
Tawil, R
Tristani-Firouzi, M
Canun, S
Bendahhou, S
Soemori, A
Donaldson, MR
Iannaccone, S
Brunt, E
Barohn, R
Clark, J
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