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Results: 3
A MOUSE MODEL FOR MITOCHONDRIAL MYOPATHY AND CARDIOMYOPATHY RESULTINGFROM A DEFICIENCY IN THE HEART MUSCLE ISOFORM OF THE ADENINE-NUCLEOTIDE TRANSLOCATOR/
Authors: GRAHAM BH WAYMIRE KG COTTRELL B TROUNCE IA MACGREGOR GR WALLACE DC
Citation: Bh. Graham et al., A MOUSE MODEL FOR MITOCHONDRIAL MYOPATHY AND CARDIOMYOPATHY RESULTINGFROM A DEFICIENCY IN THE HEART MUSCLE ISOFORM OF THE ADENINE-NUCLEOTIDE TRANSLOCATOR/, Nature genetics, 16(3), 1997, pp. 226-234
USE OF TRANSMITOCHONDRIAL CYBRIDS TO ASSIGN A COMPLEX-I DEFECT TO THEMITOCHONDRIAL DNA-ENCODED NADH DEHYDROGENASE SUBUNIT-6 GENE MUTATION AT NUCLEOTIDE PAIR-14459 THAT CAUSES LEBER HEREDITARY OPTIC NEUROPATHYAND DYSTONIA
Authors: JUN AS TROUNCE IA BROWN MD SHOFFNER JM WALLACE DC
Citation: As. Jun et al., USE OF TRANSMITOCHONDRIAL CYBRIDS TO ASSIGN A COMPLEX-I DEFECT TO THEMITOCHONDRIAL DNA-ENCODED NADH DEHYDROGENASE SUBUNIT-6 GENE MUTATION AT NUCLEOTIDE PAIR-14459 THAT CAUSES LEBER HEREDITARY OPTIC NEUROPATHYAND DYSTONIA, Molecular and cellular biology, 16(3), 1996, pp. 771-777
CYTOPLASMIC TRANSFER OF A COMPLEX-I DEFECT ASSOCIATED WITH THE MITOCHONDRIAL-DNA (MTDNA)-ENCODED ND6 NP-14459 MUTATION CAUSING LEBER HEREDITARY OPTIC NEUROPATHY AND DYSTONIA
Authors: JUN AS TROUNCE IA BROWN MD SHOFFNER JM WALLACE DC
Citation: As. Jun et al., CYTOPLASMIC TRANSFER OF A COMPLEX-I DEFECT ASSOCIATED WITH THE MITOCHONDRIAL-DNA (MTDNA)-ENCODED ND6 NP-14459 MUTATION CAUSING LEBER HEREDITARY OPTIC NEUROPATHY AND DYSTONIA, American journal of human genetics, 57(4), 1995, pp. 108-108
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