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ENJoubert Syndrome 39 (JBTS39)
Alias:
Jbts39
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Joubert Syndrome 39, is also known as jbts39. An important gene associated with Joubert Syndrome 39 is TMEM218 (Transmembrane Protein 218). Affiliated tissues include eye and liver, and related phenotypes are global developmental delay and retinal dystrophy
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MALACARDS
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