A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family.
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C. Petit | G. Lenaers | A. Barakat | C. Bonnet | M. Kandil | Aymane Bouzidi | Zied Riahi | A. Bousfiha | S. Elrharchi | M. Charif | G. Amalou
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C. Petit | G. Lenaers | A. Barakat | C. Bonnet | M. Kandil | Aymane Bouzidi | Zied Riahi | A. Bousfiha | S. Elrharchi | M. Charif | G. Amalou