학술논문 – 부산대학교 도서관

학술논문

replay검색결과 돌아가기

search검색화면

SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss

Document Type

TEXT

Author

Nesbitt, Addie I.; Tawamie, Hasan; Krantz, Ian D.; Medne, Livija; Helbig, Ingo; Matalon, Dena R.; Reis, Andre; Santani, Avni; Sticht, Heinrich; Jamra, Rami Abou; Buchert, Rebecca

Source

Subject

Language

English
German

Online Access

Open Access (Europeana)

이메일