Erratum: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations (Nature Genet. (2000) 26 (93-96))

Nature Genetics

Volumn 27, Issue 2, 2001, Pages 225-

  Hong, S E ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ERRATUM; ERROR; PRIORITY JOURNAL;

GENETTA;

EID: 0035132408     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/84886     Document Type: Erratum

References (3)

1. Genomic organization of the mouse reelin gene
2. The human reelin gene: Isolation, sequencing, and mapping on chromosome 7
3. Reln(rl-Alb2), an allele of reeler isolated from a chlorambucil screen, is due to an IAP insertion with exon skipping