The skeletal phenotype of intermediate GM1 gangliosidosis: Clinical, radiographic and densitometric features, and implications for clinical monitoring and intervention-Reference-Cited by-同舟云学术

The skeletal phenotype of intermediate GM1 gangliosidosis: Clinical, radiographic and densitometric features, and implications for clinical monitoring and intervention

Published:2020-02 Issue: Volume:131 Page:115142
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Ferreira Carlos R.,Regier Debra S.,Yoon Robin,Pan Kristen S.,Johnston Jean M.,Yang Sandra,Spranger Jürgen W.,Tifft Cynthia J.

Funder

NHGRI

National Institutes of Health

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

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3. β-Galactosidase Deficiency (β-Galactosidosis): GM1 Gangliosidosis and Morquio B Disease;Suzuki,2014

4. Human beta-galactosidase gene mutations in morquio B disease;Oshima;Am. J. Hum. Genet.,1991

5. Mucopolysaccharidosis type IVA;Regier,1993

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