Glycogen storage disease type II: identifation of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase gene

Marian Haan; D (Dik) van Leenen; J (J.) Verbiest; Arnold Reuser; MMP (Monique) Hermans

Glycogen storage disease type II: identifation of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase gene

Marian Haan, D (Dik) van Leenen, J (J.) Verbiest, Arnold Reuser, MMP (Monique) Hermans

Clinical Genetics

Research output: Contribution to journal › Article › Academic › peer-review

Original language	Undefined/Unknown
Pages (from-to)	379-382
Number of pages	4
Journal	Clinical Genetics
Volume	53
Publication status	Published - 1998

Research programs

EMC MGC-02-96-01
EMC MM-03-54-04-A

Cite this

@article{224fe7e7e6784be5ae4276fde4c11c88,

title = "Glycogen storage disease type II: identifation of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase gene",

author = "Marian Haan and {van Leenen}, {D (Dik)} and Verbiest, {J (J.)} and Arnold Reuser and Hermans, {MMP (Monique)}",

year = "1998",

language = "Undefined/Unknown",

volume = "53",

pages = "379--382",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell Publishing Ltd",

}

TY - JOUR

T1 - Glycogen storage disease type II: identifation of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase gene

AU - Haan, Marian

AU - van Leenen, D (Dik)

AU - Verbiest, J (J.)

AU - Reuser, Arnold

AU - Hermans, MMP (Monique)

PY - 1998

Y1 - 1998

M3 - Article

SN - 0009-9163

VL - 53

SP - 379

EP - 382

JO - Clinical Genetics

JF - Clinical Genetics

ER -