Phenotypic variability in a Tunisian family with X-linked...

Clinica Chimica Acta 2016 / 01 Vol. 453

Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation

Kallabi, Fakhri, Ellouz, Emna, Tabebi, Mouna, Ben Salah, Ghada, Kaabechi, Naziha, Keskes, Leila, Triki, Chahnez, Kamoun, Hassen
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Volume:
453
Language:
english
Journal:
Clinica Chimica Acta
DOI:
10.1016/j.cca.2015.12.014
Date:
January, 2016
File:
PDF, 1.31 MB
english, 2016
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