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Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia.
Rimbert A, Pichelin M, Lecointe S, Marrec M, Le Scouarnec S, Barrak E, Croyal M, Krempf M, Le Marec H, Redon R, Schott JJ, Magré J, Cariou B. Rimbert A, et al. Among authors: schott jj. Atherosclerosis. 2016 Jul;250:52-6. doi: 10.1016/j.atherosclerosis.2016.04.010. Epub 2016 Apr 11. Atherosclerosis. 2016. PMID: 27179706 Free article.
[Hereditary cardiac arrhythmia].
Le Marec H, Schott JJ. Le Marec H, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 1997 Apr;90 Spec No 1:57-66. Arch Mal Coeur Vaiss. 1997. PMID: 9238458 Review. French.
[Congenital long QT syndromes].
Le Marec H, Schott JJ. Le Marec H, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 1997 Jun;90 Spec No 3:25-35. Arch Mal Coeur Vaiss. 1997. PMID: 9295920 French.
[Genetics and cardiac arrhythmias].
Probst V, Kyndt F, Allouis M, Schott JJ, Le Marec H. Probst V, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1054-62. Arch Mal Coeur Vaiss. 2003. PMID: 14694781 Review. French.
[Genetic aspects of cardiac conduction defects].
Probst V, Kyndt F, Allouis M, Schott JJ, Le Marec H. Probst V, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1067-73. Arch Mal Coeur Vaiss. 2003. PMID: 14694782 Review. French.
150 results