A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients.

Journal

Human mutation

Journal Volume

20

Journal Issue

3

Pages

232

Date Issued

2002

Author(s)

Tang N.L.

Chan R.T.

Law L.K.

Fung L.M.

Zhang W.M.

DOI

10.1002/humu.9053

URI

https://www.scopus.com/inward/record.uri?eid=2-s2.0-18244420879&doi=10.1002%2fhumu.9053&partnerID=40&md5=b9002a6b4797d6e54a8853ec75276f72

https://scholars.lib.ntu.edu.tw/handle/123456789/526068

Type

journal article