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300263.1
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Subject Details
Country
Saudi Arabia
HPO Terms
Seizure; Intellectual disability; Motor delay; Delayed speech and language development; Hypertonia
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Sex
Male
Family History
No
Parental Consanguinity
No
Subject Variants
Variant Name
Allele Count
Associated Disease
NM_015107.3:c.1460A>G
1
Intellectual Developmental Disorder, X-Linked, Syndromic, Siderius Type
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References
Monies et al. 2017
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العربية
About Us
News
Fellowships
العربية
Home
About Us
CTGA Database
CTGA Overview
Search Database
Submit to Database
Publications
Research Articles
Genetics Made Easy
Genetic Disorders in the Arab World
Reports
Conferences & Events
News
Gallery
Fellowships
Contact Us