Mutant deoxynucleotide carrier is associated with congenital microcephaly-Reference-Cited by-同舟云学术

Mutant deoxynucleotide carrier is associated with congenital microcephaly

Published:2002-08-19 Issue:1 Volume:32 Page:175-179
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Rosenberg Marjorie J.,Agarwala Richa,Bouffard Gerard,Davis Joie,Fiermonte Giuseppe,Hilliard Mark S.,Koch Thorsten,Kalikin Linda M.,Makalowska Izabela,Morton D. Holmes,Petty Elizabeth M.,Weber James L.,Palmieri Ferdinando,Kelley Richard I.,Schäffer Alejandro A.,Biesecker Leslie G.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng948z.pdf

Reference26 articles.

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2. Dolce, V., Fiermonte, G., Runswick, M.J., Palmieri, F. & Walker, J.E. The human mitochondrial deoxynucleotide carrier and its role in the toxicity of nucleoside antivirals. Proc. Natl Acad. Sci. USA 98, 2284–2288 (2001).

3. Carey, J.C. in Rudolph's Pediatrics (eds Rudolph, A.M., Hoffman, J.I.E. & Rudolph, C.D.) 427–429 (Appleton and Lange, Stamford, CT, 1996).

4. Weber, J. & Broman, K. Genotyping for human whole-genome scans: past, present, and future. Adv. Genet. 42, 77–96 (2001).

5. Kuhlenbäumer, G. et al. A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes. Genomics 62, 242–250 (1999).

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