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Mucolipidosis type IV: the origin of the disease in the Ashkenazi Jewish population

โœ Scribed by Raas-Rothschild, Annick; Bargal, Ruth; DellaPergola, Sergio; Zeigler, Marcia; Bach, Gideon


Book ID
110024785
Publisher
Nature Publishing Group
Year
1999
Tongue
English
Weight
42 KB
Volume
7
Category
Article
ISSN
1018-4813

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๐Ÿ“œ SIMILAR VOLUMES


Mucolipidosis type IV: Novel MCOLN1 muta
โœ Ruth Bargal; Nili Avidan; Tzvia Olender; Edna Ben Asher; Marcia Zeigler; Annick ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 256 KB

The gene MCOLN1 is mutated in Mucolipidosis type IV (MLIV), a neurodegenerative, recessive, lysosomal storage disorder. The disease is found in relatively high frequency among Ashkenazi Jews due to two founder mutations that comprise 95% of the MLIV alleles in this population [Bargal et al., 2000].

The frequency of mucolipidosis type IV i
โœ Gideon Bach; Michael B.T. Webb; Ruth Bargal; Marcia Zeigler; Joseph Ekstein ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 56 KB

Mucolipidosis type IV (MLIV) is a neurodegenerative lysosomal storage disorder that occurs in an increased frequency in the Ashkenazi Jewish (AJ) population. The frequency of the disease in this population has been established by the testing of 66,749 AJ subjects in the Dor Yeshorim program, a uniqu