Barth syndrome.

Am J Med Genet C Semin Med Genet · 2013 · PMC3892174 · PMID 23843353

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may be significantno p-value reported

There are no reported genotype/phenotype correlations in BTHS and it is increasingly recognized that there may be significant intrafamilial phenotypic variability [Ronvelia et al., 2012 ].

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