Concepedia

Publication | Open Access

A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders

DOIFull Paper Access

10

Citations

14

References

2017

Year

Amale Bousfiha, Amina Bakhchane, Hicham Charoute, Zied Riahi, Khalid Snoussi, Hassan Rouba, Crystel Bonnet, Christine Petit, Abdelhamid Barakat
Human Genome Variation

References

YearCitations

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