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Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation
by
Kallabi, F., Dr
,
Ellouz, E., Dr
,
Kaabechi, N., Pr
,
Keskes, L., Pr
,
Triki, C., Pr
,
Kamoun, H., Pr
Published in
Annales d'endocrinologie
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A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with...
by
Tabebi, M
,
Mkaouar-Rebai, E., Dr
,
Mnif, M., Dr
,
Kallabi, F
,
Ben Mahmoud, A
,
Ben Saad, W., Dr
,
Charfi, N., Dr
,
Keskes-Ammar, L., Pr
,
Kamoun, H., Pr
,
Abid, M., Pr
,
Fakhfakh, F., Pr
Published in
Annales d'endocrinologie
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La déficience en enzyme HSD17B3 n’est plus une rare étiologie des 46, XY DSD dans la population tunisienne
by
Ben Rhouma, B
,
Engeli, R
,
Fakhfakh, F., Pr
,
Mnif, M., Pr
,
Kamoun, T., Pr
,
Odermatt, A., Pr
,
Kamoun, H., Pr
,
Keskes, L., Pr
,
Belguith, N., Dr
Published in
Annales d'endocrinologie
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Dysgénésies thyroïdiennes : étude du gène TSHR chez des familles du sud tunisien
by
Chaabane, R
,
Ben Ayed, I., Dr
,
Ben Rhouma, B
,
Mnif, M., Pr
,
Kamoun, T., Pr
,
Keskes, L., Pr
,
Kamoun, H., Pr
,
Belguith, N., Pr
Published in
Annales d'endocrinologie
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