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Jihen Chouchen
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Jihen Chouchen
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Jihen Chouchen
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1
Two new mutations, ESPN c.2257T>C and ESRRB c.10583 C>A, cause hearing loss in UAE families
by
Jihen
Chouchen
,
Abdelaziz Tlili
Published 2020-01-01
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Article
2
Identification of a novel OXCT1 frameshift mutation by whole-exome sequencing and evidence for nonsense-mediated mRNA decay
by
Zamzam Yousef
,
Mona Mahfood
,
Jihen
Chouchen
,
Abdullah Al Mutery
,
Abdelaziz Tlili
Published 2020-01-01
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Article
3
Whole exome sequencing, in silico and functional studies confirm the association of the GJB2 mutation p.Cys169Tyr with deafness and suggest a role for the TMEM59 gene in the hearin...
by
Mona Mahfood
,
Jihen
Chouchen
,
Walaa Kamal Eddine Ahmad Mohamed
,
Abdullah Al Mutery
,
Rania Harati
,
Abdelaziz Tlili
Published 2021-08-01
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