Reference health
Cumulative incidence rates of the mucopolysaccharidoses in Germany
17/17 checkable references clean · checked 2026-07-22
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
7 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 17 checked references that resolve
resolves10.1542/peds.105.1.e10
Incidence of Inborn Errors of Metabolism in British Columbia, 1969–1996
resolves10.1093/hmg/3.6.861
Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common α-L-iduronidase mutations (W402X and Q70X) among European patients
resolves10.1002/humu.1380060119
Mucopolysaccharidosis type I: Identification of 13 novel mutations of the α-L-iduronidase gene
resolves10.1007/s004310050685
Selective screening of 10,000 high-risk Brazilian patients for the detection of inborn errors of metabolism
resolves10.1023/B:BOLI.0000031101.12838.c6
Enzyme replacement and enhancement therapies for lysosomal diseases
resolves10.1007/BF00206770
An update on the frequency of mucopolysaccharide syndromes in British Columbia
resolves10.1007/BF00295699
Incidence of mucopolysaccharidoses in Israel: Is hunter disease a ?Jewish disease??
resolves10.1073/pnas.96.11.6296
Mutations in
<i>HYAL1</i>
, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX
resolves10.1007/s004390050656
Low β-glucuronidase enzyme activity and mutations in the human β-glucuronidase gene in mild mucopolysaccharidosis type VII, pseudodeficiency and a heterozygote
resolves10.1038/sj.ejhg.5200242
Sanfilippo type B syndrome (mucopolysaccharidosis III B): allelic heterogeneity corresponds to the wide spectrum of clinical phenotypes
resolves10.1002/humu.1189
Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications
The 7 references without a DOI — listed, not checked
no DOI — not checkedStatistical Methods in Cancer Research
no DOI — not checkedCommon language for measures of occurrence of congenital anomalies and genetic diseases: incidence or birth prevalence
no DOI — not checkedBiochemical and molecular analysis of mucopolysaccharidoses in Turkey
no DOI — not checkedLysosomal storage diseases in Greece
no DOI — not checkedESGLD Workshop
no DOI — not checkedThe Sanfilippo syndrome: a clinical and genetical study of 75 patients in The Netherlands
no DOI — not checkedMolecular analysis of patients with beta‐glucuronidase deficiency presenting as hydrops fetalis or as early mucopolysaccharidosis VII
What this badge says. CiteStamped means the CHECKABLE references of this
work were clean at the dated check: each resolved to a known work in a public registry, and none
carried a retraction notice at that time. It says nothing about the quality, findings,
or importance of the work itself, and nothing about references deposited without a DOI.
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