Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment
JACOBS, Howard T, HUTCHIN, Timothy P, ZELANTE, Leopoldo, GASPARINI, Paolo, PYYKKÖ, Ilmari, SHAH, Zahid H, ZEVIANI, Massimo, MUELLER, Robert F, KÄPPI, Timo, GILLIES, Greta, MINKKINEN, Kia, WALKER, John, THOMPSON, Karen, ROVIO, Anja T, CARELLA, Massimo, MELCHIONDA, Salvatore
Published in European journal of human genetics : EJHG (01.01.2005)
Published in European journal of human genetics : EJHG (01.01.2005)
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Journal Article
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus
Lainé, Sophie, Masmoudi, Saber, Hutchin, Tim P, Verpy, Elisabeth, Leibovici, Michel, Nouaille, Sylvie, Del Castillo, Ignacio, Blanchard, Stéphane, Petit, Christine, Popot, Jean-Luc, Moreno, Felipe, Mueller, Robert F, Zwaenepoel, Ingrid
Published in Nature genetics (01.11.2001)
Published in Nature genetics (01.11.2001)
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Journal Article
Antioxidant capacity after acute ischaemic stroke
GARIBALLA, S.E., HUTCHIN, T.P., SINCLAIR, A.J.
Published in QJM : An International Journal of Medicine (01.10.2002)
Published in QJM : An International Journal of Medicine (01.10.2002)
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Journal Article
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment
Hutchin, T P, Parker, M J, Young, I D, Davis, A C, Pulleyn, L J, Deeble, J, Lench, N J, Markham, A F, Mueller, R F
Published in Journal of medical genetics (01.09.2000)
Published in Journal of medical genetics (01.09.2000)
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Journal Article
Mitochondrial DNA Mutations in Alzheimer's Disease
Hutchin, Tim P., Heath, Paul R., Pearson, R.Carl A., Sinclair, Alan J.
Published in Biochemical and biophysical research communications (18.12.1997)
Published in Biochemical and biophysical research communications (18.12.1997)
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Journal Article
Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation
Hutchin, T P, Lench, N J, Arbuzova, S, Markham, A F, Mueller, R F
Published in European journal of human genetics : EJHG (01.01.2001)
Published in European journal of human genetics : EJHG (01.01.2001)
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Journal Article
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UK
Blaydon, DC, Mueller, RF, Hutchin, TP, Leroy, BP, Bhattacharya, SS, Bird, AC, Malcolm, S, Bitner-Glindzicz, M
Published in Clinical genetics (01.04.2003)
Published in Clinical genetics (01.04.2003)
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Journal Article
Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction
Hutchin, T P, Navarro-Coy, N C, Van Camp, G, Tiranti, V, Zeviani, M, Schuelke, M, Jaksch, M, Newton, V, Mueller, R F
Published in European journal of human genetics : EJHG (01.05.2001)
Published in European journal of human genetics : EJHG (01.05.2001)
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