Dyskinetic Movement Disorder in Congenital Methemoglobinemia Type <scp>II</scp>-Reference-Cited by-同舟云学术

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Dyskinetic Movement Disorder in Congenital Methemoglobinemia Type II

Published:2024-09-12 Issue: Volume: Page:
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Nagarajan Balamurugan¹,Gunasekaran Pradeep Kumar¹^ORCID,Anand Kiran¹,Kaushal Yashovardhan¹,Saini Arushi Gahlot¹^ORCID

Affiliation:

1. Department of Pediatrics Postgraduate Institute of Medical Education and Research Chandigarh India

Publisher

Wiley

Reference5 articles.

1. Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum

2. Recessive congenital methemoglobinemia type II: Hypoplastic basal ganglia in two siblings with a novel mutation of the cytochrome b5 reductase gene

3. A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: Determination of the molecular basis

4. Recommendations for diagnosis and treatment of methemoglobinemia

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