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Am J Hum Genet. 1998 Jan;62(1):27-35.
Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics.
Ahmanson Department of Pediatrics, Steven Spielberg Pediatric Research Center, Cedars-Sinai Medical Center and UCLA School of Medicine, Los Angeles.
PMID: 9443888 [PubMed - indexed for MEDLINE]
PMCID: PMC1376819
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Cited by 3 PubMed Central articles
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Candidate locus for a nuclear modifier gene for maternally inherited deafness.
Bykhovskaya Y, Estivill X, Taylor K, Hang T, Hamon M, Casano RA, Yang H, Rotter JI, Shohat M, Fischel-Ghodsian N.
Am J Hum Genet. 2000 Jun; 66(6):1905-10. Epub 2000 Apr 27.
[Am J Hum Genet. 2000]
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The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness.
Torroni A, Cruciani F, Rengo C, Sellitto D, López-Bigas N, Rabionet R, Govea N, López De Munain A, Sarduy M, Romero L, et al.
Am J Hum Genet. 1999 Nov; 65(5):1349-58.
[Am J Hum Genet. 1999]
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Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene.
Mansergh FC, Millington-Ward S, Kennan A, Kiang AS, Humphries M, Farrar GJ, Humphries P, Kenna PF.
Am J Hum Genet. 1999 Apr; 64(4):971-85.
[Am J Hum Genet. 1999]