Clinical and genetic findings in an unusual pedigree with infantile spinal muscular atrophy caused by a compound heterozygous mutation in the SMN1 gene (CROSBI ID 581576)
Prilog sa skupa u časopisu | sažetak izlaganja sa skupa | međunarodna recenzija
Podaci o odgovornosti
Lehman, Ivan ; Eggermann, T. ; Lochmüller, Hanns ; Sertie, J. ; Barišić, Nina
engleski
Clinical and genetic findings in an unusual pedigree with infantile spinal muscular atrophy caused by a compound heterozygous mutation in the SMN1 gene
Clinical and genetic findings in infantile spinal muscular atrophy caused by a compound heterozygous mutation in the SMN1 gene.
spinal muscular atrophy; SMN1 gene
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
Podaci o prilogu
S94-S94.
2011.
nije evidentirano
objavljeno
Podaci o matičnoj publikaciji
1090-3798
Podaci o skupu
Congress of the European Paediatric Neurology Society (9 ; 2011)
poster
11.07.2011-14.07.2011
Cavtat, Hrvatska
Povezanost rada
Kliničke medicinske znanosti
