CENPT
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Template:Short description Template:Infobox gene Centromere protein T is a protein that in humans is encoded by the CENPT gene.[1][2][3]
Clinical significance
Mutations in CENPT cause an autosomal recessive syndrome of microcephaly, short stature, skeletal abnormalities, underdeveloped genitalia and pubertal delay.[4]
See also
References
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External links
Further reading
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