Genome-wide analysis of single-nucleotide polymorphisms in human expressed sequences

K Irizarry et al.

Nature Genet. 26, 233–236 (2000).

The dbSNP accession numbers listed in the paper were incorrect. The correct accession numbers are 1508752-1556748.

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome

H van Bokhoven et al.

Nature Genet. 25, 423–426 (2000).

The designations of two of the mutations reported in this paper were not correct. The C182X mutation should be designated C182Y, and R396X should be designated R397X. The authors thank Eddy Ball (Human Mutation Database, Cardiff) for alerting them to this error.

The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development

G A Cox et al.

Nature Genet. 26, 198–202 (2000).

The last sentence of the second paragraph was incorrect, as we did not ourselves determine the sequence of human clones. The sentence as it should have read is as follows. “Very recently a partial cDNA sequence (FLJ10405) corresponding to the putative human homologue of Fi2 was deposited, as well as human BACs together comprising the entire gene (RP11-5J4, RP11-746G4), both showing 97% amino acid identity with the mouse sequence.”