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Paper Report for: Santorelli_1998_Biochem.Biophys.Res.Commun_245_519

Reference

Title: A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient
Santorelli FM, Bertini E, Petruzzella V, Di Capua M, Calvieri S, Gasparini P, Zeviani M
Ref: Biochemical & Biophysical Research Communications, 245:519, 1998 : PubMed

        



Related information

Gene_Locus| human-PPT1
Mutation | M57NfsX45_human-PPT1,



Citations formats

Santorelli FM, Bertini E, Petruzzella V, Di Capua M, Calvieri S, Gasparini P, Zeviani M (1998)
A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient
Biochemical & Biophysical Research Communications 245: 519-22

Santorelli FM, Bertini E, Petruzzella V, Di Capua M, Calvieri S, Gasparini P, Zeviani M (1998)
Biochemical & Biophysical Research Communications 245: 519-22



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