PGAP3-related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation

Journal: Clin Genet

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Year of Publication: 2018

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Abstract summary 

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Statistics
Citations :  2
Authors :  0
Identifiers
Doi : 10.1111/cge.13033
SSN : 
Study Population
Male,Female
Mesh Terms
Other Terms
Study Design
Study Approach
Country of Study
Egypt
Publication Country