Suchergebnisse - "Bax, Nathalie M"

PubPharm (35)

31

Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT)

enthalten in: Human molecular genetics | 2015

von Haer-Wigman, L. | Newman, H. | Leibu, R. | +15

32

Early-onset stargardt disease: phenotypic and genotypic characteristics

enthalten in: Ophthalmology | 2015

von Lambertus, S. | van Huet, R. | Bax, N. | +5

33

Early-Onset Stargardt Disease

enthalten in: Ophthalmology | 2015

von Lambertus, S. | van Huet, R. | Bax, N. | +5

34

The RD5000 database : facilitating clinical, genetic, and therapeutic studies on inherited retinal diseases

enthalten in: Investigative ophthalmology & visual science | 2014

von van Huet, R. | Oomen, C. | Plomp, A. | +20

35

Foveal sparing in Stargardt disease

enthalten in: Investigative ophthalmology & visual science | 2014

von van Huet, R. | Bax, N. | Westeneng-Van Haaften, S. | +7