Whole Exome Sequencing Identifies New Causative Mutations...

Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness

Riahi, Zied, Bonnet, Crystel, Zainine, Rim, Louha, Malek, Bouyacoub, Yosra, Laroussi, Nadia, Chargui, Mariem, Kefi, Rym, Jonard, Laurence, Dorboz, Imen, Hardelin, Jean-Pierre, Salah, Sihem Belhaj, Lev
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Volume:
9
Language:
french
Journal:
PLoS ONE
DOI:
10.1371/journal.pone.0099797
Date:
June, 2014
File:
PDF, 544 KB
french, 2014
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