F. Li

Identification of a Novel de Novo STK11 Mutation in a Chinese Child with Peutz-Jeghers Syndrome

R. Ai, Xiaojing Zhu, W-L Liu, 2011, The Journal of international medical research.

Characterization of a novel human putative mitochondrial transporter homologous to the yeast mitochondrial RNA splicing proteins 3 and 4

C. Larsson, B. Leibiger, I. Leibiger, 2001, FEBS letters.

Molecular analysis of the SMN gene mutations in spinal muscular atrophy patients in China.

R. Ai, F. Li, W. Liu, 2013, Genetics and molecular research : GMR.

Mapping of autosomal dominant progressive external ophthalmoplegia to a 7-cM critical region on 10q24

D. Beeson, J. Newsom-Davis, K. Morten, 1999, Neurology.

Congenital Myasthenic Syndromes: Studies of the AChR and Other Candidate Genes a

A. Vincent, D. Beeson, J. Newsom-Davis, 1998 .