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doi:10.1002/humu.23854
Human Mutation
Monica Y. Niño
Stijn L.M. in ’t Groen
Atze J. Bergsma
Nadine A.M.E. Beek
Marian Kroos
Marianne Hoogeveen‐Westerveld
Ans T. Ploeg
W.W.M. Pim Pijnappel
John Wiley & Sons, Ltd
cardiac and skeletal muscle disorder
genotype‐phenotype relationship
glycogen storage disease type II
lysosomal storage disease
www.pompecenter.nl
Human Mutation, doi:10.1002/humu.23854
10.1002/humu.23854
http://dx.doi.org/10.1002/humu.23854
journal
Human Mutation
1059-7794
VoR
John Wiley & Sons
2019-09-11T03:12:56-07:00
2019-07-27T16:38:24+05:30
2019-09-11T03:12:56-07:00
True
cardiac and skeletal muscle disorder; genotype‐phenotype relationship; glycogen storage disease type II; lysosomal storage disease; www.pompecenter.nl
iText 4.2.0 by 1T3XT
10.1002/humu.23854
10.1002/(ISSN)1098-1004
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