| Predicate | Object |
|---|---|
| rdf:type | |
| biopax3:author |
Koyama S,
Saisho S,
Shimozawa K,
Toyoura T,
Yata J
|
| biopax3:db |
PubMed
|
| biopax3:id |
12050231
|
| biopax3:source |
J Clin Endocrinol Metab 87(6);2668-73
|
| biopax3:title |
Genetic analysis of Japanese patients with 21-hydroxylase deficiency: identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients without demonstrable mutations within the structural gene for CYP21.
|
| biopax3:year |
2002
|