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{{r|Space Quest V: The Next Mutation}}

{{r|Mutation}}

{{r|Mutation}}

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...le = Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers

Some used "[[mutation]]" to refer to variations with low allele frequency. ...if a different polypeptide sequence is produced they are ''[[nonsynonymous mutation|nonsynonymous]]''.

{{r|Mutation}}

...le = Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers

...s'' is the inability to respond to vaopressin, (for instance if there is a mutation affecting the V2 vasopressin receptor) and cannot be treated in this way. ...hypothalamic diabetes insipidus is most commonly a consequence of a point mutation in the vasopressin gene, usually in the region coding for vasopressin-assoc

...//www.blackwellpublishing.com/ridley/classictexts/wright.asp "The roles of mutation, inbreeding, crossbreeding and selection in evolution"] ''Proc. 6th Int. Co

...ooks at how large scale changes may be caused by evolutionary mechanisms—[[mutation]], [[migration]], [[genetic drift]], and [[natural selection]].<ref>[http:/

Auto-populated based on [[Special:WhatLinksHere/Mutation]]. Needs checking by a human.

...h [[natural selection]] and other [[evolution]]ary processes acts. Without mutation, there are no new [[gene]]s, no new [[allele]]s and, eventually, no evoluti ...], where mutations occur up to 100 times more frequently than the normal [[mutation rate]]. A hotspot can be at an unusual base, e.g., 5-methylcytosine.

...indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Rom ...siology involving the [[voltage-gated potassium channel]]. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).."<