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Academic Journal

Increased incidence of FMO1 gene single nucleotide polymorphisms in sporadic amyotrophic lateral sclerosis.

  • Authors : Cereda C; Experimental Neurobiology, Neurological Institute IRCCS C Mondino, Pavia, Italy. ; Gabanti E

Subjects: Amyotrophic Lateral Sclerosis/Amyotrophic Lateral Sclerosis/Amyotrophic Lateral Sclerosis/*epidemiology ; Amyotrophic Lateral Sclerosis/Amyotrophic Lateral Sclerosis/Amyotrophic Lateral Sclerosis/*genetics ; Oxygenases/Oxygenases/Oxygenases/*genetics

  • Source: Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases [Amyotroph Lateral Scler] 2006 Dec; Vol. 7 (4), pp. Publisher: Informa Healthcare Country of Publication: England NLM ID: 101283386 Publication Model: Print Cited Medium: Print ISSN: 1748-2968

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Alkaptonuria in Italy: polymorphic haplotype background, mutational profile, and description of four novel mutations in the homogentisate 1,2-dioxygenase gene.

Subjects: Dioxygenases*; Alkaptonuria/Alkaptonuria/Alkaptonuria/*genetics ; Oxygenases/Oxygenases/Oxygenases/*genetics

  • Source: Journal of medical genetics [J Med Genet] 2000 Apr; Vol. 37 (4), pp. 309-12.Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print Cited Medium: Print ISSN:

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  • 1-10 of  38 results for ""Oxygenases""