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FAM46A mutations are responsible for autosomal recessive osteogenesis imperfecta.
J Med Genet. 2018 Apr;55(4):278-284. doi: 10.1136/jmedgenet-2017-104999. Epub 2018 Jan 22.
J Med Genet. 2018.
PMID: 29358272
Maternal uniparental disomy of chromosome 2 in a patient with a DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome.
Haudry C, de Lonlay P, Malan V, Bole-Feysot C, Assouline Z, Pruvost S, Brassier A, Bonnefont JP, Munnich A, Rötig A, Lebre AS.
Haudry C, et al.
Mol Genet Metab. 2012 Dec;107(4):700-4. doi: 10.1016/j.ymgme.2012.10.008. Epub 2012 Oct 22.
Mol Genet Metab. 2012.
PMID: 23141463
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New SUCLG1 patients expanding the phenotypic spectrum of this rare cause of mild methylmalonic aciduria.
Valayannopoulos V, Haudry C, Serre V, Barth M, Boddaert N, Arnoux JB, Cormier-Daire V, Rio M, Rabier D, Vassault A, Munnich A, Bonnefont JP, de Lonlay P, Rötig A, Lebre AS.
Valayannopoulos V, et al. Among authors: haudry c.
Mitochondrion. 2010 Jun;10(4):335-41. doi: 10.1016/j.mito.2010.02.006. Epub 2010 Mar 1.
Mitochondrion. 2010.
PMID: 20197121
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