Maroteaux-Lamy syndrome in a large consanguineous kindred: Biochemical and immunological studies

Author:

Black Susan H.,Pelias Mary Z.,Miller James B.,Blitzer Miriam G.,Shapira Emmanuel,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Reference18 articles.

1. A distinct biochemical deficit in the maroteaux-lamy syndrome (mucopolysaccharidosis VI)

2. (1974): Abstracts of the Civil Records of St. Charles Parish 1700-1803. The U.S. L. History Series, Lafayette, LA.

3. (1969): “The Settlement of the German Coast of Louisiana and the Creoles of German descent.” Baltimore: Genealogical Publishing Co.

4. Is multiple sulphatase deficiency due to defective regulation of sulphohydrolase expression?

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice;Journal of Bone and Mineral Research;2021-05-10

2. Mucopolysaccharidosis VI;Atlas of Genetic Diagnosis and Counseling;2012

3. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991

4. Inborn errors of complex carbohydrate metabolism;American Journal of Medical Genetics;1987-10

5. Mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome);Atlas of Genetic Diagnosis and Counseling

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