DOI: 10.1055/s-00043281

Journal of Neurosciences in Rural Practice

References

Kammoun JellouliN, Salem IH, Ellouz E, Louhichi N, tlili A, Kammoun F. et al.
Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease.

Gene 2013;
513: 233-8

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