A novel delins (c.773_819+47delinsAA) mutation of the PCCA gene associated with neonatal-onset propionic acidemia: a case report | BMC Medical Genetics | Full Text
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A novel delins (c.773_819+47delinsAA) mutation of the PCCA gene associated with neonatal-onset propionic acidemia: a case report | BMC Medical Genetics | Full Text
A Novel Delins Mutation in the α-TTP Gene in a Family Segregating Ataxia With Isolated Vitamin E Deficiency | Pediatric Research
![PDF] A Novel Delins Mutation in the α-TTP Gene in a Family Segregating Ataxia With Isolated Vitamin E Deficiency | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5c9db32adbc0022d3ef7b06ca882a5c82bb0571d/2-Figure1-1.png "PDF] A Novel Delins Mutation in the α-TTP Gene in a Family Segregating Ataxia With Isolated Vitamin E Deficiency | Semantic Scholar")
PDF] A Novel Delins Mutation in the α-TTP Gene in a Family Segregating Ataxia With Isolated Vitamin E Deficiency | Semantic Scholar
