Validation of a targeted gene panel sequencing for the diagnosis of hereditary chronic liver diseases.

Saved in:

Bibliographic Details
Title:	Validation of a targeted gene panel sequencing for the diagnosis of hereditary chronic liver diseases.
Authors:	Ronzoni L; Biological Resource Centre, Precision Medicine Lab, Transfusion Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy., Marini I; Biological Resource Centre, Precision Medicine Lab, Transfusion Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy., Passignani G; Biological Resource Centre, Precision Medicine Lab, Transfusion Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy., Malvestiti F; Department of Pathophysiology and Transplantation, Università Degli Studi di Milano, Milano, Italy., Marchelli D; Biological Resource Centre, Precision Medicine Lab, Transfusion Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy., Bianco C; Biological Resource Centre, Precision Medicine Lab, Transfusion Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy., Pelusi S; Biological Resource Centre, Precision Medicine Lab, Transfusion Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy., Prati D; Biological Resource Centre, Precision Medicine Lab, Transfusion Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy., Valenti L; Biological Resource Centre, Precision Medicine Lab, Transfusion Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy.; Department of Pathophysiology and Transplantation, Università Degli Studi di Milano, Milano, Italy.
Source:	Frontiers in genetics [Front Genet] 2023 Jun 14; Vol. 14, pp. 1137016. Date of Electronic Publication: 2023 Jun 14 (Print Publication: 2023).
Publication Type:	Journal Article
Journal Info:	Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1664-8021
DOI:	10.3389/fgene.2023.1137016