Girl with signs of Pelizaeus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference22 articles.
1. Autosomal recessive form of connatal Pelizaeus-Merzbacher disease
2. Pelizaeus-Merzbacher disease: identification of heterozygotes with magnetic resonance imaging?
3. Pelizaeus-Merzbacher Disease: Clinical and Nosological Study
4. Connatal Pelizaeus-Merzbacher disease: An autosomal recessive form
5. Myelin mosaicism in female heterozygotes of the canine shaking pup and myelin-deficient rat mutants
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