Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

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  137. Montrer des auteurs +
Revue:
American Journal of Medical Genetics, Part A

ISSN: 1552-4833 1552-4825

Année de publication: 2015

Volumen: 167

Número: 2

Pages: 296-312

Type: Article

DOI: 10.1002/AJMG.A.36887 GOOGLE SCHOLAR

Objectifs de Développement Durable