Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Moncef Kheirallah"'
Autor:
Zied Riahi, Crystel Bonnet, Rim Zainine, Saida Lahbib, Yosra Bouyacoub, Rym Bechraoui, Jihène Marrakchi, Jean-Pierre Hardelin, Malek Louha, Leila Largueche, Salim Ben Yahia, Moncef Kheirallah, Leila Elmatri, Ghazi Besbes, Sonia Abdelhak, Christine Petit
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120584 (2015)
Usher syndrome (USH) is an autosomal recessive disorder characterized by combined deafness-blindness. It accounts for about 50% of all hereditary deafness blindness cases. Three clinical subtypes (USH1, USH2, and USH3) are described, of which USH1 is
Externí odkaz:
https://doaj.org/article/a1cec40889d2405db2ba7c181f4782b6
Autor:
Sonia Abdelhak, Zied Riahi, L. Largueche, Rim Zainine, Moncef Kheirallah, Leila Elmatri, Christine Petit, Ghazi Besbes, Saida Lahbib, Yosra Bouyacoub, J. Marrakchi, Crystel Bonnet, Jean-Pierre Hardelin, Salim Ben Yahia, Rym Bechraoui, Malek Louha
Publikováno v:
PLoS ONE
PLoS ONE, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
PLoS ONE, Public Library of Science, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
PLoS ONE, Vol 10, Iss 3, p e0120584 (2015)
PLoS ONE, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
PLoS ONE, Public Library of Science, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
PLoS ONE, Vol 10, Iss 3, p e0120584 (2015)
International audience; Usher syndrome (USH) is an autosomal recessive disorder characterized by combined deafness-blindness. It accounts for about 50% of all hereditary deafness blindness cases. Three clinical subtypes (USH1, USH2, and USH3) are des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49896b9629524498a57fde1557d4de8a
https://hal-pasteur.archives-ouvertes.fr/pasteur-01221041/document
https://hal-pasteur.archives-ouvertes.fr/pasteur-01221041/document