P.12.10 Exome sequencing analysis reveals a mutation of...

Neuromuscular Disorders 2013 / 10 Vol. 23; Iss. 9-10

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.
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.592
Date:
October, 2013
File:
PDF, 48 KB
english, 2013
Conversion to is in progress
Conversion to is failed