Bo Jin
Nanjing, 210008, China
Last Updated: 09/26/2026
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Found 8 publications
Early-onset ophthalmoplegia, cervical dyskinesia, and lower extremity weakness due to partial deletion of chromosome 16: A case report.
Journal: World journal of clinical cases
Published: March 25, 2022
Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.
Journal: Orphanet journal of rare diseases
Published: May 07, 2021
Candida meningitis in an infant after abdominal surgery successfully treated with intrathecal and intravenous amphotericin B: A case report.
Journal: Medicine
Published: April 20, 2021
Analysis of a child with megalencephalic leukoencephalopathy with subcortical cyst type 2B caused by HEPACAM variant
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 27, 2020
Identification of a missense ARSA mutation in metachromatic leukodystrophy and its potential pathogenic mechanism.
Journal: Molecular genetics & genomic medicine
Published: February 06, 2020
Rapamycin inhibits peritoneal fibrosis by modifying lipid homeostasis in the peritoneum.
Journal: American journal of translational research
Published: October 17, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026