Mitochondrial T9957C Mutation in Association with NAION and Seizures but not MELAS

By Abu-Amero Khaled   Bosley Thomas   Bohlega Saeed   Hansen Erik  

Ophthalmic Genetics, Vol. 26, Iss. 1, 2005-03 ,pp. : 31-36

Informa Healthcare

Access to resources Recommend Favorite

Phylogenetic Assessment of the Mitochondrial DNA Displacement Loop Haplotype in Japanese Patients with Leber’s Hereditary Optic Neuropathy Harboring the Mitochondrial DNA G11778A Mutation

By  

Ophthalmic Research, Vol. 35, Iss. 4, 2003-06 ,pp. : 224-231

Karger

Access to resources Recommend Favorite

Prevalence and audiological characteristics in individuals with auditory neuropathy/auditory dys-synchrony

By Kumar U. Ajith   Jayaram M. M.  

International Journal of Audiology, Vol. 45, Iss. 6, 2006-06 ,pp. : 360-366

Informa Healthcare

Access to resources Recommend Favorite

Brazilian young adults and noise: Attitudes, habits, and audiological characteristics

By Zocoli Angela Maria Fontana   Morata Thais Catalani   Marques Jair Mendes   Corteletti Lilian Jacob  

International Journal of Audiology, Vol. 48, Iss. 10, 2009-10 ,pp. : 692-699

Informa Healthcare

Access to resources Recommend Favorite

Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations

By Ali Mahmood   Venkatesh Conjeevaram   Ragunath Anitha   Kumar Arun  

Ophthalmic Genetics, Vol. 25, Iss. 4, 2004-12 ,pp. : 247-255

Informa Healthcare

Access to resources Recommend Favorite