Literature DB >> 28148224

Erratum to: Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome.

Zahraa Haidar¹, Ramzi Temanni², Eliane Chouery¹, Puthen Jithesh², Wei Liu³, Rashid Al-Ali², Ena Wang³, Francesco M Marincola⁴, Nadine Jalkh¹, Soha Haddad⁵, Wassim Haidar⁶, Lotfi Chouchane⁷, André Mégarbané⁸.

Abstract

Entities: Disease

Year: 2017 PMID： 28148224 PMCID： PMC5286771 DOI： 10.1186/s12863-017-0480-z

Source DB: PubMed Journal: BMC Genet ISSN： 1471-2156 Impact factor: 2.797

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Erratum

Shortly after the publication of this article [1], one of the authors noticed that his name had been misspelled. The article has been updated. ‘Puthen Jitesh’ has been changed to ‘Puthen Jithesh’.

1 in total

1. Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome.

Authors: Zahraa Haidar; Ramzi Temanni; Eliane Chouery; Puthen Jithesh; Wei Liu; Rashid Al-Ali; Ena Wang; Francesco M Marincola; Nadine Jalkh; Soha Haddad; Wassim Haidar; Lotfi Chouchane; André Mégarbané
Journal: BMC Genet Date: 2017-01-19 Impact factor: 2.797

1 in total

1. The combined prevalence of classified rare rheumatic diseases is almost double that of ankylosing spondylitis.

Authors: Judith Leyens; Tim Th A Bender; Martin Mücke; Christiane Stieber; Dmitrij Kravchenko; Christian Dernbach; Matthias F Seidel
Journal: Orphanet J Rare Dis Date: 2021-07-22 Impact factor: 4.123

1 in total