P.12.10 Exome sequencing analysis reveals a mutation of Kir3.4 in a patient with Andersen–Tawil syndrome

✍ Scribed by 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.

• Book ID: 123465513
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 48 KB
• Volume: 23
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2013.06.592