[cite web | title = Entrez Gene: CYTB cytochrome b| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4519| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
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*cite journal | author=Maca-Meyer N, González AM, Larruga JM, "et al." |title=Major genomic mitochondrial lineages delineate early human expansions. |journal=BMC Genet. |volume=2 |issue= |pages= 13 |year= 2003 |pmid= 11553319 |doi=
*cite journal | author=Herrnstadt C, Elson JL, Fahy E, "et al." |title=Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups. |journal=Am. J. Hum. Genet. |volume=70 |issue= 5 |pages= 1152–71 |year= 2002 |pmid= 11938495 |doi=
*cite journal | author=Silva WA, Bonatto SL, Holanda AJ, "et al." |title=Mitochondrial genome diversity of Native Americans supports a single early entry of founder populations into America. |journal=Am. J. Hum. Genet. |volume=71 |issue= 1 |pages= 187–92 |year= 2002 |pmid= 12022039 |doi=
*cite journal | author=Yamasoba T, Goto Y, Oka Y, "et al." |title=Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene. |journal=Neuromuscul. Disord. |volume=12 |issue= 5 |pages= 506–12 |year= 2002 |pmid= 12031626 |doi=
*cite journal | author=Mishmar D, Ruiz-Pesini E, Golik P, "et al." |title=Natural selection shaped regional mtDNA variation in humans. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=100 |issue= 1 |pages= 171–6 |year= 2003 |pmid= 12509511 |doi= 10.1073/pnas.0136972100
*cite journal | author=Mancuso M, Filosto M, Stevens JC, "et al." |title=Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene. |journal=J. Neurol. Sci. |volume=209 |issue= 1-2 |pages= 61–3 |year= 2003 |pmid= 12686403 |doi=
*cite journal | author=Ingman M, Gyllensten U |title=Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines. |journal=Genome Res. |volume=13 |issue= 7 |pages= 1600–6 |year= 2003 |pmid= 12840039 |doi= 10.1101/gr.686603
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*cite journal | author=Maca-Meyer N, González AM, Pestano J, "et al." |title=Mitochondrial DNA transit between West Asia and North Africa inferred from U6 phylogeography. |journal=BMC Genet. |volume=4 |issue= |pages= 15 |year= 2004 |pmid= 14563219 |doi= 10.1186/1471-2156-4-15
*cite journal | author=Haut S, de Villemeur TB, Brivet M, "et al." |title=The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers. |journal=Eur. J. Hum. Genet. |volume=12 |issue= 3 |pages= 220–4 |year= 2004 |pmid= 14735157 |doi= 10.1038/sj.ejhg.5201132
*cite journal | author=Palanichamy MG, Sun C, Agrawal S, "et al." |title=Phylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South Asia. |journal=Am. J. Hum. Genet. |volume=75 |issue= 6 |pages= 966–78 |year= 2005 |pmid= 15467980 |doi= 10.1086/425871
*cite journal | author=Starikovskaya EB, Sukernik RI, Derbeneva OA, "et al." |title=Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups. |journal=Ann. Hum. Genet. |volume=69 |issue= Pt 1 |pages= 67–89 |year= 2005 |pmid= 15638829 |doi= 10.1046/j.1529-8817.2003.00127.x
*cite journal | author=Rajkumar R, Banerjee J, Gunturi HB, "et al." |title=Phylogeny and antiquity of M macrohaplogroup inferred from complete mt DNA sequence of Indian specific lineages. |journal=BMC Evol. Biol. |volume=5 |issue= 1 |pages= 26 |year= 2006 |pmid= 15804362 |doi= 10.1186/1471-2148-5-26
*cite journal | author=Thangaraj K, Chaubey G, Kivisild T, "et al." |title=Reconstructing the origin of Andaman Islanders. |journal=Science |volume=308 |issue= 5724 |pages= 996 |year= 2005 |pmid= 15890876 |doi= 10.1126/science.1109987
*cite journal | author=Blakely EL, Mitchell AL, Fisher N, "et al." |title=A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast. |journal=FEBS J. |volume=272 |issue= 14 |pages= 3583–92 |year= 2005 |pmid= 16008558 |doi= 10.1111/j.1742-4658.2005.04779.x
*cite journal | author=Kivisild T, Shen P, Wall DP, "et al." |title=The role of selection in the evolution of human mitochondrial genomes. |journal=Genetics |volume=172 |issue= 1 |pages= 373–87 |year= 2006 |pmid= 16172508 |doi= 10.1534/genetics.105.043901
*cite journal | author=Behar DM, Metspalu E, Kivisild T, "et al." |title=The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event. |journal=Am. J. Hum. Genet. |volume=78 |issue= 3 |pages= 487–97 |year= 2006 |pmid= 16404693 |doi= 10.1086/500307
*cite journal | author=van Holst Pellekaan SM, Ingman M, Roberts-Thomson J, Harding RM |title=Mitochondrial genomics identifies major haplogroups in Aboriginal Australians. |journal=Am. J. Phys. Anthropol. |volume=131 |issue= 2 |pages= 282–94 |year= 2006 |pmid= 16596590 |doi= 10.1002/ajpa.20426
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