6 results on '"Ait-Kaci, M."'
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2. C.P.2.10 A patient with RSMD1 associated with the particular SEPN1 c.G872A mutation
3. Clinical and pathological study of 80 patients with muscular dystrophy in Algeria
4. P.P.7 04 A homozygous COL6A1 splice site mutation in siblings with Ullrich congenital muscular dystrophy
5. P.P.1 04 Algerian FKRP mutations causing MDC1C congenital muscular dystrophy with mental retardation
6. Isotope effect in the predissociation of the c4Σu-state of O+2
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