Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation-Reference-Cited by-同舟云学术

Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation

Published:1998-06-05 Issue:5 Volume:77 Page:421-426
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bykhovskaya Yelena,Shohat Mordechai,Ehrenman Karen,Johnson David,Hamon Melanie,Cantor Rita M.,Aouizerat Bradley,Bu Xiangdong,Rotter Jerome I.,Jaber Lutfi,Fischel-Ghodsian Nathan

Publisher

Wiley

Subject

Genetics(clinical)

Reference22 articles.

1. Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome

2. Audiovestibular Findings in Patients With Deafness Caused by a Mitochondrial Susceptibility Mutation and Precipitated by an Inherited Nuclear Mutation or Aminoglycosides

3. Two-locus mitochondrial and nuclear gene models for mitochondrial disorders

4. Leber’s Hereditary Optic Neuroretinopathy and the X-Chromosomal Susceptibility Factor: No Linkage to DXS7

5. Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12S rRNA gene: Evidence of heteroplasmy

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