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Molecular Genetic Analysis of Tunisian Patients with a Clas..:
Kharrat, Maher
;
Tardy, Véronique
;
M'Rad, Ridha
...
The Journal of Clinical Endocrinology & Metabolism. 89 (2004) 1 - p. 368-374 , 2004
Link:
https://doi.org/10.1210/jc.2003-031056
RT Journal T1
Molecular Genetic Analysis of Tunisian Patients with a Classic Form of 21-Hydroxylase Deficiency: Identification of Four Novel Mutations and High Prevalence of Q318X Mutation
UL https://suche.suub.uni-bremen.de/peid=cr-10.1210_jc.2003-031056&Exemplar=1&LAN=DE A1 Kharrat, Maher A1 Tardy, Véronique A1 M'Rad, Ridha A1 Maazoul, Faouzi A1 Jemaa, Lamia Ben A1 Refaï, Mohamed A1 Morel, Yves A1 Chaabouni, Habiba PB The Endocrine Society YR 2004 SN 0021-972X SN 1945-7197 JF The Journal of Clinical Endocrinology & Metabolism VO 89 IS 1 SP 368 OP 374 LK http://dx.doi.org/https://doi.org/10.1210/jc.2003-031056 DO https://doi.org/10.1210/jc.2003-031056 SF ELIB - SuUB Bremen
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