Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/131/3/760/903096/awm337.pdf
Cited by 59 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemia;Clinica Chimica Acta;2025-01
2. Dyskinetic Movement Disorder in Congenital Methemoglobinemia Type II;Movement Disorders Clinical Practice;2024-09-12
3. Novel Compound Heterogeneous Mutations in <i>CYB5R3</i> Gene Leading to Methemoglobinemia (Type I) in a Chinese Boy: Case Report and Relevant Comprehensive Analysis;Acta Haematologica;2024-05-24
4. Recessive Hereditary Methemoglobinemia Type II in a Microcephalic Infant;Clinical Pediatrics;2024-03-04
5. METHEMOGLOBINEMIA WITH NEUROLOGICAL MANIFESTATIONS: A CASE OF RECESSIVE CONGENITAL METHEMOGLOBINEMIA TYPE II;Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi;2024-01-12
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