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pro vyhledávání: '"Marianna Herrera"'
Autor:
Claudia Carranza, Guney Bademci, Marianna Herrera, Majid Mojarrad, M'hamed Grati, Joseph Foster, Abhiraami Kannan-Sundhari, Yong Feng, Denise Yan, F. Basak Cengiz, Mariem Bensaid, Akeem O. Lasisi, Reza Maroofian, Saber Masmoudi, Alex M. Mawla, Mahdiyeh Behnam, Bing Zou, Duygu Duman, Rahul Mittal, Demet Tekin, Mohan Kameswaran, Waheed A. Adedeji, Xuezhong Liu, Rosemary I. Kabahuma, Alexander Nord, Mustafa Tekin, T.J. Lasisi, Andrew H. Crosby, Susan H. Blanton, Ibis Menéndez, Shengru Guo
Publikováno v:
Human genetics, vol 135, iss 8
Hearing loss is the most common sensory deficit in humans with causative variants in over 140 genes. With few exceptions, however, the population-specific distribution for many of the identified variants/genes is unclear. Until recently, the extensiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40d9d35b96efcfd3f46fd9900fa5371b
https://doi.org/10.1007/s00439-016-1697-z
https://doi.org/10.1007/s00439-016-1697-z
