Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia-Reference-Cited by-同舟云学术

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia

Published:2009-05-03 Issue:6 Volume:41 Page:651-653
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Guernsey Duane L,Jiang Haiyan,Campagna Dean R,Evans Susan C,Ferguson Meghan,Kellogg Mark D,Lachance Mathieu,Matsuoka Makoto,Nightingale Mathew,Rideout Andrea,Saint-Amant Louis,Schmidt Paul J,Orr Andrew,Bottomley Sylvia S,Fleming Mark D,Ludman Mark,Dyack Sarah,Fernandez Conrad V,Samuels Mark E

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.359.pdf

Reference14 articles.

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2. Fleming, M.D. Semin. Hematol. 39, 270–281 (2002).

3. Bottomley, S.S., May, B.K., Cox, T.C., Cotter, P.D. & Bishop, D.F. J. Bioenerg. Biomembr. 27, 161–168 (1995).

4. Camaschella, C. Br. J. Haematol. 143, 27–38 (2008).

5. Palmieri, F. et al. Biochim. Biophys. Acta 1757, 1249–1262 (2006).

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