Connexin43 mutations in sporadic and familial defects of laterality

N Engl J Med. 1995 Oct 5;333(14):941; author reply 941-2.

Authors

M P Splitt, J Burn, J Goodship

PMID: 7666890

No abstract available

Publication types

Comment
Letter

MeSH terms

Connexin 43 / genetics*
DNA
Heart Defects, Congenital / genetics
Humans
Nuclear Family
Point Mutation*
Situs Inversus / genetics*

Substances

Connexin 43
DNA