Reply to Bandelt et al [2]

European Journal of Human Genetics

Volumn 15, Issue 4, 2007, Pages 402-404

  Martorell, Lourdes ^a   Vilella, Elisabet ^a  

^a IISPV   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; NUCLEOTIDE;

DNA DETERMINATION; DNA SEQUENCE; GENE DELETION; GENETIC DATABASE; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; LETTER; NUCLEOTIDE SEQUENCE; PARKINSON DISEASE; PATHOPHYSIOLOGY; PHYLOGENY; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SCHIZOPHRENIA; SEQUENCE ANALYSIS; SPECTROPHOTOMETRY;

EID: 33947666083     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201782     Document Type: Letter

References (4)

1. Huerta C, Castro MG, Coto E et al: Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population. J Neurol Sci 2005; 236: 49-54.
2. Andrews RM, Kubacka I, Chinnery PF et al: Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet 1999; 23: 147.
3. Bandelt H-J, Richards M, Macaulay V (eds): Human mitochondrial DNA and the evolution of Homo sapiens. Series: Nucleic Acids and Molecular Biology, vol. 18, Springer-Verlag: Berlin-Heidelberg, 2006.
4. Bandelt H-J, Salas A, Bravi CM: What is a 'novel' mtDNA mutation - and does 'novelty' really matter? J Hum Genet 2006; 51: 1073-1082.