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keywords > Genetic Phenomena > Founder Effect
The adaptation rate of asexuals: deleterious mutations, clonal interference and population bottlenecks.
L239F founder mutation in GDAP1 is associated with a mild Charcot-Marie-Tooth type 4C4 (CMT4C4) phenotype.
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.