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P.12.10 Exome sequencing analysis reveals a mutation of Kir3.4 in a patient with Andersen–Tawil syndrome
Kokunai, Y., Nakamori, M., Kubota, T., Mochizuki, H., Takahashi, M.P., Nakata, T., Ohno, K., Sakata, S., Okamura, Y., Kimura, H., Itoh, H., Horie, M., Osaki, Y., Shindo, K.Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.592
Date:
October, 2013
File:
PDF, 48 KB
english, 2013