Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mokhtar Hasbelaoui"'
Autor:
Samia Abdi, Amel Bahloul, Asma Behlouli, Jean-Pierre Hardelin, Mohamed Makrelouf, Kamel Boudjelida, Malek Louha, Ahmed Cheknene, Rachid Belouni, Yahia Rous, Zahida Merad, Djamel Selmane, Mokhtar Hasbelaoui, Crystel Bonnet, Akila Zenati, Christine Petit
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0161893 (2016)
Usher syndrome (USH) is an autosomal recessive disorder characterized by a dual sensory impairment affecting hearing and vision. USH is clinically and genetically heterogeneous. Ten different causal genes have been reported. We studied the molecular
Externí odkaz:
https://doaj.org/article/cdd7c7d5a2624b7981550dfab526b138
Autor:
Amel Bahloul, Zahida Merad, Yahia Rous, Christine Petit, Mokhtar Hasbelaoui, Jean-Pierre Hardelin, Kamel Boudjelida, Akila Zenati, Ahmed Cheknene, Rachid Belouni, Malek Louha, Crystel Bonnet, Samia Abdi, Asma Behlouli, Mohamed Makrelouf, Djamel Selmane
Publikováno v:
PLoS ONE
PLoS ONE, 2016, 11 (9), pp.e0161893. ⟨10.1371/journal.pone.0161893⟩
PLoS ONE, Public Library of Science, 2016, 11 (9), pp.e0161893. ⟨10.1371/journal.pone.0161893⟩
PLoS ONE, Vol 11, Iss 9, p e0161893 (2016)
PLoS ONE, 2016, 11 (9), pp.e0161893. ⟨10.1371/journal.pone.0161893⟩
PLoS ONE, Public Library of Science, 2016, 11 (9), pp.e0161893. ⟨10.1371/journal.pone.0161893⟩
PLoS ONE, Vol 11, Iss 9, p e0161893 (2016)
International audience; Usher syndrome (USH) is an autosomal recessive disorder characterized by a dual sensory impairment affecting hearing and vision. USH is clinically and genetically heterogeneous. Ten different causal genes have been reported. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ea54c606eaea9abe9ba77ba2a724d57
https://hal.sorbonne-universite.fr/hal-01388303/document
https://hal.sorbonne-universite.fr/hal-01388303/document
