Mutations in the CEP290 %25252528NPHP6%25252529 gene are a f…
Mutations in the CEP290 %25252528NPHP6%25252529 gene are a frequent cause of Leber congenital amaurosis.
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Elsevier ScienceDirect Journals
Coverage:
- 1997-06~present
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Cell Press
Coverage:
- 1997-06~present
Collection:
PubMed Central
Coverage:
- 1949~6 months ago