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2008 | 2 |
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Mutations in MAFA and IAPP are not a common cause of monogenic diabetes.
Diabet Med. 2009 Jul;26(7):746-8. doi: 10.1111/j.1464-5491.2009.02758.x.
Diabet Med. 2009.
PMID: 19573128
No abstract available.
Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients.
Garin I, Rica I, Estalella I, Oyarzabal M, Rodríguez-Rigual M, San Pedro JI, Pérez-Nanclares G, Fernández-Rebollo E, Busturia MA, Castaño L, Pérez de Nanclares G; Spanish MODY Group.
Garin I, et al.
Clin Endocrinol (Oxf). 2008 Jun;68(6):873-8. doi: 10.1111/j.1365-2265.2008.03214.x. Epub 2008 Feb 1.
Clin Endocrinol (Oxf). 2008.
PMID: 18248649
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Heterozygous glucokinase mutations and birth weight in Spanish children.
de Las Heras J, Martínez R, Rica I, de Nanclares GP, Vela A, Castaño L; Spanish MODY group.
de Las Heras J, et al.
Diabet Med. 2010 May;27(5):608-10. doi: 10.1111/j.1464-5491.2010.02953.x.
Diabet Med. 2010.
PMID: 20536962
No abstract available.
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[Cardiovascular risk in subjects with high probability of metabolic syndrome and insulin resistance. DESIRE study].
Goday A, Gabriel R, Ascaso JF, Franch J, Ortega R, Martínez O, Lerones N; DESIRE study.
Goday A, et al.
Rev Clin Esp. 2008 Sep;208(8):377-85. doi: 10.1157/13126339.
Rev Clin Esp. 2008.
PMID: 18817695
Spanish.
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