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Items: 7

1.

Mitochondrial tRNA-serine (AGY) m.C12264T mutation causes severe multisystem disease with cataracts.

Schrier SA, Wong LJ, Place E, Ji JQ, Pierce EA, Golden J, Santi M, Anninger W, Falk MJ.

Discov Med. 2012 Feb;13(69):143-50.

2.

Mitochondrial Disorders Overview.

Chinnery PF.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2000 Jun 8 [updated 2014 Aug 14].

3.

MELAS.

DiMauro S, Hirano M.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2001 Feb 27 [updated 2013 Nov 21].

4.

MERRF.

DiMauro S, Hirano M.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2003 Jun 3 [updated 2015 Jan 29].

5.

Mitochondrial DNA Deletion Syndromes.

DiMauro S, Hirano M.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2003 Dec 17 [updated 2011 May 3].

6.

Protean manifestations of mitochondrial diseases: a minireview.

Kerr DS.

J Pediatr Hematol Oncol. 1997 Jul-Aug;19(4):279-86. Review.

PMID:
9256824
7.
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