Journal of Pediatric Genetics

LinksSchließen

Referenz

Soda H, Yukizane S, Yoshida I, Koga Y, Aramaki S, Kato H.
A point mutation in exon 3 (His 107-->Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement.

Hum Genet 1996;
97 (04) 435-437

Bibliographische Angaben herunterladen

Aufrufen in: