Hypochondroplasia with Acanthosis Nigricans and Moyamoya Disease
Author:
Funder
Pusan National University Hospital
Publisher
The Korean Child Neurology Society
Subject
Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Link
http://annchildneurol.org/upload/pdf/acn-2022-00402.pdf
Reference10 articles.
1. Acanthosis Nigricans: A practical approach to evaluation and management
2. Familial Acanthosis Nigricans Due to K650T FGFR3 Mutation
3. Distinct Missense Mutations of the FGFR3 Lys650 Codon Modulate Receptor Kinase Activation and the Severity of the Skeletal Dysplasia Phenotype
4. Acanthosis nigricans in a Chinese girl with FGFR3 K650 T mutation: a case report and literature review
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