Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency (vol 8, pg 655, 1999)

Tang, NLS Ganapathy, V Wu, X Hui, J Seth, P Yuen, PMP Wanders, RJA Fok, TF Hjelm, NM

Nls. Tang et al., Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency (vol 8, pg 655, 1999), HUM MOL GEN, 8(5), 1999, pp. 943-943

1

Molecular Biology & Genetics

HUMAN MOLECULAR GENETICS

09646906 → ACNP

8

5

1999

943 - 943

ISI

0964-6906(199905)8:5<943:MOOAOC>2.0.ZU;2-K