A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

Michael A. Whitney, Hiroshi Saito, Petra M. Jakobs, Rachel A. Gibson, Robb E. Moses, Markus Grompe

Research output: Contribution to journalArticle

121 Scopus citations

Abstract

Fanconi anaemia is an autosomal recessive disease for which four known complementation groups exist. Recently, the gene defective in complementation group C (FACC) has been cloned. In order to determine the fraction of Fanconi anaemia caused by FACC mutations, we used reverse transcription PCR and chemical mismatch cleavage (CMC) to examine the FACC cDNA in 17 FA cell lines. 4/17 patients (23.5%) had mutations in this gene. Two Ashkenazi–Jewish individuals were homozygous for an identical splice mutation. Three additional Jewish patients bearing this allele were found upon screening 21 other families. We conclude that a common mutation in FACC accounts for the majority of Fanconi anaemia in Ashkenazi–Jewish families.

Original languageEnglish (US)
Pages (from-to)202-205
Number of pages4
JournalNature genetics
Volume4
Issue number2
DOIs
StatePublished - Jun 1993

ASJC Scopus subject areas

  • Genetics

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