Novel mutation in the methyltransferase domain of DNMT1 in a hereditary sensory and autonomic neuropathy patient with hearing loss, cataract, and dementia
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T. Kanda | H. Takashima | H. Nishihara | M. Koga | M. Kawai | A. Hashiguchi | Junhui Yuan | Y. Higuchi | M. Omoto | J. Ogasawara