The 208delG mutation in FSCN2 does not associate with retinal degeneration in Chinese individuals (Q34605952)

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The 208delG mutation in FSCN2 does not associate with retinal degeneration in Chinese individuals
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    The 208delG mutation in FSCN2 does not associate with retinal degeneration in Chinese individuals (English)
    1 February 2007

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