ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.

Brain · 2016 · PMC5839554 · PMID 26556829

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borderline significantno p-value reported

All other ARCMT2 pedigrees with heterozygous haplotypes had a negative or borderline significant cumulative logarithm of odds score by the genetic program HOMOG ( Ott, 1983 ).

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