Author/Creator: Fratter, C - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Fratter, C

1. Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease. Issue 10 (19th September 2011)

Authors:: Uusimaa, J; Jungbluth, H; Fratter, C; Crisponi, G; Feng, L; Zeviani, M; Hughes, I; Treacy, E P; Birks, J; Brown, G K; Sewry, C A; McDermott, M; Muntoni, F; Poulton, J
Journal:: Journal of medical genetics
Issue:: Volume 48:Issue 10(2011)
Page Start:: 660
Record Type:: Journal Article
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2. POG04 Multiple mitochondrial DNA deletions, cyclooxygenase-negative fibres and slowly progressive cognitive decline with psychiatric features. Issue 11 (22nd October 2010)

Authors:: Rajakulendran, S; Pitceathly, R D S; Warren, J; Woodward, C; Sweeney, M G; Hargreaves, I; Fratter, C; Heales, S; Taylor, R; Holton, J L; Rahman, S; Hanna, M G
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 81:Issue 11(2010)
Page Start:: e49
Record Type:: Journal Article
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3. Information for genetic management of mtDNA disease: sampling pathogenic mtDNA mutants in the human germline and in placenta. Issue 4 (12th November 2009)

Authors:: Marchington, D; Malik, S; Banerjee, A; Turner, K; Samuels, David; Macaulay, V; Oakeshott, P; Fratter, C; Kennedy, S; Poulton, J
Journal:: Journal of medical genetics
Issue:: Volume 47:Issue 4(2010)
Page Start:: 257
Record Type:: Journal Article
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