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Spectrum, frequency, and genotype–phenotype of mutations in SPATA7
PURPOSE: To describe the mutation spectrum of SPATA7 and associated ocular phenotypes. METHODS: As part of a continuing examination of the genetic basis of inherited ophthalmic diseases, sequencing variations in SPATA7 were identified in sequencing data from 5,090 probands. Mutations in SPATA7 were...
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| Gepubliceerd in: | Mol Vis |
|---|---|
| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Molecular Vision
2019
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6925664/ https://ncbi.nlm.nih.gov/pubmed/31908400 |
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