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A novel missense mutation of GJA8 causes congenital cataract in a large Mauritanian family.
Eur J Ophthalmol. 2019 Nov;29(6):621-628. doi: 10.1177/1120672118804757. Epub 2018 Oct 29.
Eur J Ophthalmol. 2019.
PMID: 30373400
Free article.
Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma.
Hadrami M, Bonnet C, Zeitz C, Veten F, Biya M, Hamed CT, Condroyer C, Wang P, Sidi MM, Cheikh S, Zhang Q, Audo I, Petit C, Houmeida A.
Hadrami M, et al.
Mol Vis. 2019 Jul 13;25:373-381. eCollection 2019.
Mol Vis. 2019.
PMID: 31367175
Free PMC article.
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HLA class I (-A, -B, -C) and class II (-DR, -DQ) polymorphism in the Mauritanian population.
Hamed CT, Meiloud G, Veten F, Hadrami M, Ghaber SM, Boussaty EC, Habti N, Houmeida A.
Hamed CT, et al. Among authors: hadrami m.
BMC Med Genet. 2018 Jan 3;19(1):2. doi: 10.1186/s12881-017-0514-4.
BMC Med Genet. 2018.
PMID: 29298671
Free PMC article.
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Some of the amino acid chemistry going on in the Laboratory of Amino Acids, Peptides and Proteins.
Bouifraden S, Drouot C, el Hadrami M, Guenoun F, Lecointe L, Mai N, Paris M, Pothion C, Sadoune M, Sauvagnat B, Amblard M, Aubagnac JL, Calmes M, Chevallet P, Daunis J, Enjalbal C, Fehrentz JA, Lamaty F, Lavergne JP, Lazaro R, Rolland V, Roumestant ML, Viallefont P, Vidal Y, Martinez J.
Bouifraden S, et al. Among authors: el hadrami m.
Amino Acids. 1999;16(3-4):345-79. doi: 10.1007/BF01388176.
Amino Acids. 1999.
PMID: 10399020
Review.
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