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Items: 4

1.
X-linked recessive inheritance of sensorineural hearing loss expressed during adolescence.
L P Pelletier, R B Tanguay
Am J Hum Genet. 1975 Sep; 27(5): 609–613.
PMCID:
PMC1762819
SummaryPage BrowsePDF–436K
2.
A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
L Tranebjaerg, C Schwartz, H Eriksen, S Andreasson, V Ponjavic, A Dahl, R E Stevenson, M May, F Arena, D Barker, et al.
J Med Genet. 1995 Apr; 32(4): 257–263. doi: 10.1136/jmg.32.4.257
PMCID:
PMC1050371
SummaryPage BrowsePDF–1.2M
3.
Mitochondria and dystonia: The movement disorder connection?
Douglas C. Wallace, Deborah G. Murdock
Proc Natl Acad Sci U S A. 1999 Mar 2; 96(5): 1817–1819. doi: 10.1073/pnas.96.5.1817
PMCID:
PMC33525
ArticlePDF–128K
4.
Human deafness dystonia syndrome is a mitochondrial disease
Carla M. Koehler, Danielle Leuenberger, Sabeeha Merchant, Anja Renold, Tina Junne, Gottfried Schatz
Proc Natl Acad Sci U S A. 1999 Mar 2; 96(5): 2141–2146. doi: 10.1073/pnas.96.5.2141
PMCID:
PMC26750
AbstractArticlePDF–352K

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