H. Suzuki

Distribution and frequencies of CDH23 mutations in Japanese patients with non‐syndromic hearing loss

Y. Takumi, S. Usami, M. Wagatsuma, 2007, Clinical genetics.

An oral CD40 ligand gene therapy against lymphoma using attenuated Salmonella typhimurium.

M. Urashima, Y. Yuza, M. Akiyama, 2000, Blood.

NOVEL COMPOUND HETEROZYGOUS ALS2 MUTATIONS CAUSE JUVENILE AMYOTROPHIC LATERAL SCLEROSIS IN JAPAN

H. Miyajima, S. Kono, T. Ohashi, 2009, Neurology.

Galactosylceramide and galactosylsphingosine loading studies in cultured skin fibroblasts in human and murine globoid cell leukodystrophy.

Y. Eto, H. Ida, H. Suzuki, 1990, Biochemical and biophysical research communications.

A novel point mutation in the gene encoding capillary morphogenesis protein 2 in a Japanese patient with juvenile hyaline fibromatosis

H. Suzuki, A. Hatamochi, T. Sasaki, 2007, The British journal of dermatology.

Pfeiffer syndrome caused by haploinsufficient mutation of FGFR2.

Y. Eto, H. Suzuki, M. Tsukuno, 1999, Journal of craniofacial genetics and developmental biology.

p53 mutations in non-small cell lung cancer in Japan: association between mutations and smoking.

R. Ueda, Takashi Takahashi, T. Takahashi, 1992, Cancer research.

[Impaired cholesterol esterification in Niemann-Pick disease model mouse].

Y. Eto, K. Maekawa, H. Suzuki, 1991, No to hattatsu = Brain and development.