Journal of Pediatric Genetics

LinksSchließen

Referenz

Shah GN, Bonapace G, Hu PY, Strisciuglio P, Sly WS.
Carbonic anhydrase II deficiency syndrome (osteopetrosis with renal tubular acidosis and brain calcification): novel mutations in CA2 identified by direct sequencing expand the opportunity for genotype-phenotype correlation.

Hum Mutat 2004;
24 (03) 272

Bibliographische Angaben herunterladen

Aufrufen in: