Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness (Q21090614)
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- Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness
| Language | Label | Description | Also known as |
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| English | Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness |
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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness (English)
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Christine Petit
Christine
Petit
Sonia Abdelhak
Sonia
Abdelhak
Jean-Pierre Hardelin
Jean-Pierre
Hardelin
Kenneth
McElreavey
Kenneth McElreavey
Zied Riahi
Rim Zainine
Malek Louha
Yosra Bouyacoub
Rym Kefi
Laurence Jonard
Imen Dorboz
Sihem Belhaj Salah
Jacqueline Levilliers
Dominique Weil
Odile Tanguy Boespflug
Ghazi Besbes
2014
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9
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6
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e99797
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13 June 2014
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