PTRH2 gene mutation causes progressive congenital skeletal muscle pathology

Bibliographic Details
Title: PTRH2 gene mutation causes progressive congenital skeletal muscle pathology
Authors: Doe, J., Jijiwa, M., de la Vega, M., Hu, H., Griffiths, G. S., Fontelonga, T. M., Barraza, P., Cruz, V., Van Ry, P., Ramos, J. W.
Source: HUMAN MOLECULAR GENETICS. 26(8):1458-1464
Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN384509804&indx=1&recIds=ETOCRN384509804
Database: British Library Document Supply Centre Inside Serials & Conference Proceedings
More Details
ISSN:09646906
Published in:HUMAN MOLECULAR GENETICS
Language:English