Work

Analyses of gene mutation, clinical phenotype, treatment and follow up of 10 cases with chronic infantile neurologic, cutaneous, articular syndrome

Year: 2019

Type: article

Study design: Case Report

Source: Zhonghua fengshibingxue zazhi

DOI: 10.3760/cma.j.issn.1007-7480.2019.08.007

Authors: Junmei Zhang, Caifeng Li, Xiaohua Tan, Yurong Piao, Tongxin Han, Weiying Kuang, Jiang Wang, Jianghong Deng, Chao Li

Institutions: Capital Medical University, Beijing Children’s Hospital

Language: English

Topic: Inflammasome and immune disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W3029131815

FWCI:

Cites:

Cited by: 2

Related to: 10