Clinical, biochemical and molecular characterization of prosaposin deficiency-Reference-Cited by-同舟云学术

Clinical, biochemical and molecular characterization of prosaposin deficiency

Author:

Motta M.¹,Tatti M.²,Furlan F.³,Celato A.³,Di Fruscio G.⁴⁵,Polo G.³,Manara R.³,Nigro V.⁴⁵,Tartaglia M.¹,Burlina A.³,Salvioli R.²

Affiliation:

1. Genetics and Rare Diseases Research Division; Ospedale Pediatrico Bambino Gesù; Rome Italy

2. Department of Haematology, Oncology and Molecular Medicine; Istituto Superiore di Sanità; Rome Italy

3. Division of Inherited Metabolic Diseases; University Hospital; Padua Italy

4. Department of Biochemistry, Biophysics and General Pathology; Second University of Naples; Naples Italy

5. Telethon Institute of Genetics and Medicine (TIGEM); Naples Italy

Funder

Associazione COMETA-ASMME (Associazione Studio Malattie Metaboliche Ereditarie)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference32 articles.

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