Hearing loss in fabry disease: A 16 year follow-up study of the Danish nationwide cohort.

Journal Information

Full Title: Mol Genet Metab Rep

Abbreviation: Mol Genet Metab Rep

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Genetics & Heredity

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

Transparency Score
3/6
50.0% Transparent
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Evidence found in paper:

"Declaration of Competing Interest U·F-R. has received Advisory Board honoraria from Amicus Therapeutics, Freeline Therapeutics, 10.13039/100013995Sanofi Genzyme, and Takeda, speaker honoraria from Amicus Therapeutics, 10.13039/100013995Sanofi Genzyme, and Takeda, grant support from 10.13039/100007343Shire and 10.13039/100013995Sanofi Genzyme, and is a member of the European Advisory Board of the Fabry and FollwMe Registries."

Evidence found in paper:

"Ira Hagen Pedersen (Nurse), Anne Marie Jensen (Audiological technical officer), Erik Finn Kjærbøl (M.Sc. E. E.) and Casper Kok (laboratory technician) are thanked for excellent assistance. Members of the Fabry Team at Rigshospitalet are thanked for continuously supplying data. UFR's research salary was supported by the Kirsten and Freddy Johansen's Fund. The project was financially supported by 10.13039/100004339Sanofi-Genzyme."

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Open Access
Paper is freely available to read
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Last Updated: Aug 05, 2025