María de la Luz Arenas‐Sordo

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Güney Bademci, Joseph Foster, Nejat Mahdieh et al. · Genetics in Medicine · 2015 · 159 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Megalencephalic leukoencephalopathy with subcortical cysts

Eline M. Hamilton, Pınar Tektürk, Fia Cialdella et al. · Neurology · 2018 · 81 citations · Full text

Medicine, Neurology, Neuroscience +9

Novel pathogenic variants underlie SLC26A4 -related hearing loss in a multiethnic cohort

Filiz Başak Cengiz, Rasim Yılmazer, Levent Olgun et al. · International Journal of Pediatric Otorhinolaryngology · 2017 · 26 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Unique spectrum of GJB2 mutations in Mexico

María de la Luz Arenas‐Sordo, Ibis Menéndez, Edgar Hernández‐Zamora et al. · International Journal of Pediatric Otorhinolaryngology · 2012 · 20 citations

Life Sciences, Genetics, Molecular Genetics +12

Cockayne's syndrome: a case report. Literature review.

María de la Luz Arenas‐Sordo, Edgar Hernández‐Zamora, Luis Alberto Montoya-Pérez et al. · PubMed · 2006 · 19 citations

Life Sciences, Genetics, Molecular Genetics +17