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De novo EEF1A2 mutations in patients with characteristic facial features, intellectual disability, autistic behaviors and epilepsy
Nakajima, J., Okamoto, N., Tohyama, J., Kato, M., Arai, H., Funahashi, O., Tsurusaki, Y., Nakashima, M., Kawashima, H., Saitsu, H., Matsumoto, N., Miyake, N.Volume:
87
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12394
Date:
April, 2015
File:
PDF, 1.22 MB
english, 2015