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disease
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MRT42 (Mental retardation, autosomal recessive 42; 精神遅滞, 常染色体劣性42)
JCEG ID
Family
Name
Locus Tag
Human Ortholog Name
OMIM
GWAS Catalog
JCEG062
*
=
GPI-anchor synthesis
T19B10.8
PGAP1
611655
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