Khalil et al., 2021 - Google Patents
Research Article Variant Analysis of Alkaptonuria Families with Significant Founder Effect in JordanKhalil et al., 2021
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- 16794841966321679564
- Author
- Khalil R
- Ali D
- Mwafi N
- Alsaraireh A
- Obeidat L
- Albsoul E
- Al Sbou I
- Publication year
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Snippet
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 …
- 206010001689 Alkaptonuria 0 title abstract description 47
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