Yamamoto, S., Okuhara, K., Tonoki, H., Iizuka, S., Nihei, N., & Tajima, T. (2013). A Novel Deletion Mutation of SLC16A2 Encoding Monocarboxylate Transporter (MCT) 8 in a 26-year-old Japanese Patient with Allan-Herndon-Dudley Syndrome. The Japanese Society for Pediatric Endocrinology.

Yamamoto, Sayaka, Koji Okuhara, Hidefumi Tonoki, Susumu Iizuka, Noriko Nihei, a Toshihiro Tajima. A Novel Deletion Mutation of SLC16A2 Encoding Monocarboxylate Transporter (MCT) 8 in a 26-year-old Japanese Patient With Allan-Herndon-Dudley Syndrome. The Japanese Society for Pediatric Endocrinology, 2013.

Yamamoto, Sayaka, et al. A Novel Deletion Mutation of SLC16A2 Encoding Monocarboxylate Transporter (MCT) 8 in a 26-year-old Japanese Patient With Allan-Herndon-Dudley Syndrome. The Japanese Society for Pediatric Endocrinology, 2013.