Large-Scale Screening of Mitochondrial DNA Mutations Among Iranian Patients with Prelingual Nonsyndromic Hearing Impairment

Dna Mutations ◽

Large Scale Screening ◽

Iranian Patients

Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment

Biochemical and Biophysical Research Communications ◽

10.1016/j.bbrc.2009.05.083 ◽

2009 ◽

Vol 385 (3) ◽

pp. 445-448 ◽

Cited By ~ 19

Author(s):

Seema Bhalla ◽

Rajni Sharma ◽

Gaurav Khandelwal ◽

Naresh K. Panda ◽

Madhu Khullar

Keyword(s):

Mitochondrial Dna ◽

Hearing Impairment ◽

Dna Mutations ◽

Indian Patients ◽

Low Incidence ◽

Syndromic Hearing Impairment

Leber’s Hereditary Optic Neuropathy: The Spectrum of Mitochondrial DNA Mutations in Iranian Patients

Mitochondrial Pathogenesis ◽

10.1007/978-3-662-41088-2_35 ◽

2004 ◽

pp. 345-349

Author(s):

Massoud Houshmand ◽

F. Sharifpanah ◽

A. Tabasi ◽

M.-H. Sanati ◽

M. Vakilian ◽

...

Keyword(s):

Mitochondrial Dna ◽

Optic Neuropathy ◽

Leber’S Hereditary Optic Neuropathy ◽

Leber's Hereditary Optic Neuropathy ◽

Dna Mutations ◽

Hereditary Optic Neuropathy ◽

Iranian Patients

Leber's Hereditary Optic Neuropathy: The Spectrum of Mitochondrial DNA Mutations in Iranian Patients

Annals of the New York Academy of Sciences ◽

10.1196/annals.1293.035 ◽

2004 ◽

Vol 1011 (1) ◽

pp. 345-349 ◽

Cited By ~ 12

Author(s):

M HOUSHMAND ◽

F SHARIFPANAH ◽

A TABASI ◽

M-H SANATI ◽

M VAKILIAN ◽

...

Keyword(s):

Mitochondrial Dna ◽

Optic Neuropathy ◽

Leber’S Hereditary Optic Neuropathy ◽

Leber's Hereditary Optic Neuropathy ◽

Dna Mutations ◽

Hereditary Optic Neuropathy ◽

Iranian Patients

Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment

Journal of Medical Genetics ◽

10.1136/jmg.38.4.229 ◽

2001 ◽

Vol 38 (4) ◽

pp. 229-231 ◽

Cited By ~ 30

Author(s):

T P Hutchin

Keyword(s):

Mitochondrial Dna ◽

Hearing Impairment ◽

Sensorineural Hearing ◽

Dna Mutations ◽

Sensorineural Hearing Impairment

Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment

European Journal of Human Genetics ◽

10.1038/sj.ejhg.5201250 ◽

2004 ◽

Vol 13 (1) ◽

pp. 26-33 ◽

Cited By ~ 85

Author(s):

Howard T Jacobs ◽

Timothy P Hutchin ◽

Timo Käppi ◽

Greta Gillies ◽

Kia Minkkinen ◽

...

Keyword(s):

Mitochondrial Dna ◽

Hearing Impairment ◽

Mitochondrial DNA Mutations in Aging, Disease and Cancer

10.1007/978-3-662-12509-0 ◽

1998 ◽

Cited By ~ 26

Keyword(s):

Mitochondrial Dna ◽

The Effect of Mitochondrial DNA Mutations in Brain Tumors

Journal of Basic and Clinical Health Sciences ◽

10.30621/jbachs.2019.590 ◽

2019 ◽

Author(s):

Zübeyde Erbayraktar ◽

Zeynep Haşimoğlu ◽

R. Serhat Erbayraktar

Keyword(s):

Mitochondrial Dna ◽

Brain Tumors ◽

Faculty Opinions recommendation of Pathogenic mitochondrial DNA mutations are common in the general population.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1119462.577067 ◽

2008 ◽

Author(s):

Nereo Bresolin ◽

Dario Ronchi

Keyword(s):

Mitochondrial Dna ◽

General Population ◽

Faculty Opinions recommendation of Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.14417.471920 ◽

2006 ◽

Author(s):

Giancarlo Vecchio

Keyword(s):

Mitochondrial Dna ◽

Oxidative Phosphorylation ◽

Oncocytic Carcinoma ◽

Faculty Opinions recommendation of Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.719010746.793534247 ◽

2017 ◽

Author(s):

Martijn Huynen

Keyword(s):

Mitochondrial Dna ◽

Human Cancer ◽

Dna Mutations ◽

Functional Consequences