Article

Detection of in rs876657372 (delACGT) in PRSS12 Gene, Risk Factors and Associated Congenital Abnormalities in Non-Syndromic Intellectual Disability-Case Control Study.

2020-10-07

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold><italic>PRSS12</italic> gene was the first gene to be identified as a cause of a non-syndromic autosomal recessive form of intellectual disability (ID). A 4-base pair deletion (delACGT; rs876657372) in the <italic>PRSS12</italic> gene has been detected in two different families diagnosed with autosomal recessive non-syndromic intellectual disability (NS-ID). Here...

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Literature Corpus work: 24440fbf-72e1-5e6c-b971-17729a67aed4
DOI: 10.21203/rs.3.rs-51237/v1

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Detection of in rs876657372 (delACGT) in PRSS12 Gene, Risk Factors and Associated Congenital Abnormalities in Non-Syndromic Intellectual Disability-Case Control Study.DOI 10.21203/rs.3.rs-51237/v1Read

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