Identification of a Novel Mutation (867delA) in the Glucose-6-phosphatase Gene in Two Siblings with Glycogen Storage Disease Type Ia with Different Phenotypes

Jan Peter Rake*, Annelies M. ten Berge, Gepke Visser, Edwin Verlind, Klary E. Niezen-Koning, Charles H. C. M. Buys, G. Peter A. Smit, Hans Scheffer

*Corresponding author voor dit werk

OnderzoeksoutputAcademicpeer review

10 Citaten (Scopus)

Samenvatting

We identified a novel mutation (867delA) in the glucose-6-phosphatase gene of two siblings with glycogen storage disease type Ia. Although both siblings share the same mutations, their phenotype regarding adult height and hepatomegaly differs. In glycogen storage disease type Ia, substantial heterogeneity in phenotype is observed. Till so far, no evidence for a clear genotype-phenotype correlation has been found. (C) 2000 Wiley-Liss, Inc.

Originele taal-2English
Pagina's (van-tot)381-U23
Aantal pagina's3
TijdschriftHuman Mutation
Volume15
Nummer van het tijdschrift4
DOI's
StatusPublished - apr.-2000

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