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Finally, mutations were ignored because we analyze the situation in which recombination is the dominant source of genetic variation (the model incorporating mutations is described in Additional file 1 under 'Effect of finite populations').
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Mutations were described in brackets.
List of genes in which mutations were described to affect the leptin-melanocortin signaling pathway [3, 6, 7, 9, 20, 36 46].
Unless noted otherwise, mutations were described previously [43].
All these mutations were described in association with hyperglycemia.
Numerous reverse transcriptase and protease mutations were described in the viral sequence of these patients.
The PHO5 UASp2, Uand2 and TATA box mutations were described previously [8], [29].
Details of sequencing results for mutations are described in Table 4.
Although most of these mutations have been described, the details of construction for some of the mutations are described here for the first time.
Rex coat mutations were described in cats [1],[2], rats [3],[4], mice [5] (several mutations), and rabbits [6].
Mutations are described using HGVS nomenclature and the positions of mutations and predicted pathogenic events are reported with respect to reference sequence NM_004006.2 for the Dp427m isoform.
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