Neil Howell
MitoKor Inc.
12780 High Bluff Drive
Suite 210
San Diego
USA
Name/email consistency: high
- Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigree. Howell, N., Kubacka, I., Keers, S.M., Turnbull, D.M., Chinnery, P.F. Hum. Genet. (2005)
- African Haplogroup L mtDNA sequences show violations of clock-like evolution. Howell, N., Elson, J.L., Turnbull, D.M., Herrnstadt, C. Mol. Biol. Evol. (2004)
- The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates. Howell, N., Smejkal, C.B., Mackey, D.A., Chinnery, P.F., Turnbull, D.M., Herrnstadt, C. Am. J. Hum. Genet. (2003)
- Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy. Howell, N., Oostra, R.J., Bolhuis, P.A., Spruijt, L., Clarke, L.A., Mackey, D.A., Preston, G., Herrnstadt, C. Am. J. Hum. Genet. (2003)
- Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background. Howell, N., Herrnstadt, C., Shults, C., Mackey, D.A. Am. J. Med. Genet. A (2003)
- LHON and other optic nerve atrophies: the mitochondrial connection. Howell, N. Dev. Ophthalmol (2003)
- Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutations. Howell, N., Miller, N.R., Mackey, D.A., Arnold, A., Herrnstadt, C., Williams, I.M., Kubacka, I. J. Neuroophthalmol (2002)
