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TSC2, 4-BP DEL, IVS20, +1

National Institutes of Health

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1 relation
TUBEROUS SCLEROSIS 2 (disorder)

Papers overview

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2019
2019
Mutation analysis of FBN1 gene in two Chinese families with congenital ectopia lentis in northern China.
AIM To summarize the phenotypes and identify the underlying genetic cause of the fibrillin-1 (FBN1) gene responsible for… 
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