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Khalil et al., 2021 - Google Patents

Research Article Variant Analysis of Alkaptonuria Families with Significant Founder Effect in Jordan

Khalil et al., 2021

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Document ID
16794841966321679564
Author
Khalil R
Ali D
Mwafi N
Alsaraireh A
Obeidat L
Albsoul E
Al Sbou I
Publication year

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Background. Metabolic disorder alkaptonuria is an autosomal recessive disorder caused by mutations in the HGD gene, and a deficiency HGD enzyme activity results in an accumulation of homogentisic acid (HGA), ochronosis, and destruction of connective tissue …
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