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[Recommendations for aminoacids chromatography analysis].
Veauville A, Acquaviva-Bourdain C, Nowoczyn M, Read MH, Corne C, Dessein AF, Van Noolen L, Garnotel R, Minet-Quinard R. Veauville A, et al. Among authors: read mh. Ann Biol Clin (Paris). 2020 Oct 1;78(5):555-564. doi: 10.1684/abc.2020.1585. Ann Biol Clin (Paris). 2020. PMID: 33026350 Free article. French.
[Down syndrome maternal serum screening: results' comments recommended by accredited biologists].
Muller F, Dreux S, Czerkiewicz I, Bernard M, Guibourdenche J, Lacroix I, Moineau MP, Read MH, Sault C, Thibaud D, Veyrat B; ABA; Bidat L. Muller F, et al. Among authors: read mh. J Gynecol Obstet Biol Reprod (Paris). 2014 Nov;43(9):671-9. doi: 10.1016/j.jgyn.2014.05.012. Epub 2014 Sep 11. J Gynecol Obstet Biol Reprod (Paris). 2014. PMID: 25218268 French.
Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria.
Nota B, Struys EA, Pop A, Jansen EE, Fernandez Ojeda MR, Kanhai WA, Kranendijk M, van Dooren SJ, Bevova MR, Sistermans EA, Nieuwint AW, Barth M, Ben-Omran T, Hoffmann GF, de Lonlay P, McDonald MT, Meberg A, Muntau AC, Nuoffer JM, Parini R, Read MH, Renneberg A, Santer R, Strahleck T, van Schaftingen E, van der Knaap MS, Jakobs C, Salomons GS. Nota B, et al. Among authors: read mh. Am J Hum Genet. 2013 Apr 4;92(4):627-31. doi: 10.1016/j.ajhg.2013.03.009. Am J Hum Genet. 2013. PMID: 23561848 Free PMC article.
A novel mutation 3090 G>A of the mitochondrial 16S ribosomal RNA associated with myopathy.
Coulbault L, Deslandes B, Herlicoviez D, Read MH, Leporrier N, Schaeffer S, Mouadil A, Lombès A, Chapon F, Jauzac P, Allouche S. Coulbault L, et al. Among authors: read mh. Biochem Biophys Res Commun. 2007 Oct 26;362(3):601-5. doi: 10.1016/j.bbrc.2007.08.040. Epub 2007 Aug 15. Biochem Biophys Res Commun. 2007. PMID: 17761147
30 results