Matches in Nanopublications for { ?s ?p "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_assertion description "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.
- assertion description "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP792653.RASXVLoobsfxvX9HBZYoKZZ1OHAXezjiFiUDN7kSyxGTA130_assertion description "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792653.RASXVLoobsfxvX9HBZYoKZZ1OHAXezjiFiUDN7kSyxGTA130_provenance.
- assertion description "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP353092.RALq_K8iGhoWdB9OBgjgk2jCF2y2N42Z1Qnqq6AlVtDmQ130_assertion description "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353092.RALq_K8iGhoWdB9OBgjgk2jCF2y2N42Z1Qnqq6AlVtDmQ130_provenance.
- NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_assertion description "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_provenance.
- NP451959.RA0hoTi3jsZrtC0fCbXGEqnRsYv06vNQjJw_wQgygwZ_U130_assertion description "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451959.RA0hoTi3jsZrtC0fCbXGEqnRsYv06vNQjJw_wQgygwZ_U130_provenance.