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P J Lamont

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Neuropediatrics|November 10, 2004
Nemaline rods and complex I deficiency in three infants with hypotonia, motor delay and failure to thriveP J Lamont, D R Thorburn, V Fabian, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 2005
Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsyP J Lamont, B Udd, F L Mastaglia, et al.
Neuromuscular Disorders : NMD|July 13, 2012
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvementT Cullup, P J Lamont, S Cirak, et al.
American Journal of Human Genetics|April 17, 1999
An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathyK M Clark, R W Taylor, M A Johnson, et al.
Acta Neuropathologica Communications|March 3, 2019
Altered myogenesis and premature senescence underlie human TRIM32-related myopathyE Servián-Morilla, M Cabrera-Serrano, E Rivas-Infante, et al.
Neurogastroenterology and Motility|May 22, 2018
Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstructionG Ravenscroft, S Pannell, G O'Grady, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Neuropediatrics|November 10, 2004
Nemaline rods and complex I deficiency in three infants with hypotonia, motor delay and failure to thriveP J Lamont, D R Thorburn, V Fabian, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 2005
Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsyP J Lamont, B Udd, F L Mastaglia, et al.
Neuromuscular Disorders : NMD|July 13, 2012
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvementT Cullup, P J Lamont, S Cirak, et al.
American Journal of Human Genetics|April 17, 1999
An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathyK M Clark, R W Taylor, M A Johnson, et al.
Acta Neuropathologica Communications|March 3, 2019
Altered myogenesis and premature senescence underlie human TRIM32-related myopathyE Servián-Morilla, M Cabrera-Serrano, E Rivas-Infante, et al.
Neurogastroenterology and Motility|May 22, 2018
Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstructionG Ravenscroft, S Pannell, G O'Grady, et al.
Pageof 2