Seung-Taek Lee

发表

Novel and recurrent mutations of the LDL receptor gene in Korean patients with familial hypercholesterolemia.

Jong-Won Kim, Ji-Hyun Kim, Jeong-Ho Kim, 2004, Molecules and cells.

DNA-based prenatal diagnosis of a Korean family with tyrosinase-related oculocutaneous albinism (OCA1)

Sang-Kyu Park, Jin-Sung Lee, Y. Park, 1997, Japanese Journal of Human Genetics.

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

R. Spritz, B. Horsthemke, R. Nicholls, 1993, Nature.

Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)

R. Spritz, D. Chitayat, K. Brøndum‐Nielsen, 1997, Human mutation.

Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele.

R. Spritz, M. Butler, R. Nicholls, 1997, American journal of medical genetics.

Organization and sequence of the human P gene and identification of a new family of transport proteins.

R. Spritz, R. Nicholls, S. T. Lee, 1995, Genomics.

Complementation of hypopigmentation in p-mutant (pink-eyed dilution) mouse melanocytes by normal human P cDNA, and defective complementation by OCA2 mutant sequences.

R. Spritz, D. Bennett, E. Sviderskaya, 1997, The Journal of investigative dermatology.

Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism.

R. Spritz, R. Laxová, R. Nicholls, 1994, The New England journal of medicine.

Diverse mutations of the P gene among African-Americans with type II (tyrosinase-positive) oculocutaneous albinism (OCA2).

E. Zackai, N. Spinner, R. Spritz, 1994, Human molecular genetics.

A survey of protein tyrosine kinase mRNAs expressed in normal human melanocytes.

R. Spritz, S. T. Lee, K. Strunk, 1993, Oncogene.