Cite
HARVARD Citation
Pihlstrøm, L. et al. (n.d.). Effective Variant Detection by Targeted Deep Sequencing of DNA Pools: An Example from Parkinson's Disease. Annals of human genetics. pp. 243-252. [Online].
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Pihlstrøm, L. et al. (n.d.). Effective Variant Detection by Targeted Deep Sequencing of DNA Pools: An Example from Parkinson's Disease. Annals of human genetics. pp. 243-252. [Online].