SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis.

Brain · 2010 · PMC2822627 · PMID 20110243

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slightly significantno p-value reported

The other ARJALS families (RM306 and TK005) showed heterozygous haplotypes and produced negative or slightly significant cumulative logarithm of odds scores by the genetic program HOMOG (data not shown) (Ott, 1983 ).

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