The African origin of the common mutation in African American patients with glycogen-storage disease type II [3]

J. A. Becker, J. Vlach, N. Raben, K. Nagaraju, E. M. Adams, M. M. Hermans, A. J J Reuser, S. S. Brooks, C. J. Tifft, R. Hirschhorn, M. L. Huie, M. Nicolino, P. H. Plotz

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)991-994
Number of pages4
JournalAmerican Journal of Human Genetics
Volume62
Issue number4
DOIs
StatePublished - 1998
Externally publishedYes

ASJC Scopus subject areas

  • Genetics

Cite this

Becker, J. A., Vlach, J., Raben, N., Nagaraju, K., Adams, E. M., Hermans, M. M., Reuser, A. J. J., Brooks, S. S., Tifft, C. J., Hirschhorn, R., Huie, M. L., Nicolino, M., & Plotz, P. H. (1998). The African origin of the common mutation in African American patients with glycogen-storage disease type II [3]. American Journal of Human Genetics, 62(4), 991-994. https://doi.org/10.1086/301788