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Article

Novel genetic mutations responsible for the HPRT deficiency and the clinical phenotypes in Japanese.

Advances in experimental medicine and biology - 1 Jan 2000

Yamada Y, Nomura N, Kitoh H, Wakamatsu N, Ogasawara N

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PMID: 11783502
DOI: 10.1007/0-306-46843-3_6

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