Abstract
The association of diseases with genes is complex, even among mendelian disorders. A new study shows that mutations in the gene encoding filamin B (FLNB) cause four distinct disorders of human skeletal development.
Cite
CITATION STYLE
APA
Biesecker, L. G. (2004, April). Phenotype matters. Nature Genetics. https://doi.org/10.1038/ng0404-323
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free