Wikidata

(Q34605952)

English

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

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title
The 208delG mutation in FSCN2 does not associate with retinal degeneration in Chinese individuals (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17251446
retrieved
3 August 2017
publication date
1 February 2007
1 reference
stated in
Europe PubMed Central
PubMed ID
17251446
retrieved
3 August 2017

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