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Links from PMC

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MBTPS2
(W226L)
Single nucleotide variant
(missense variant)
IFAP syndrome 1, with or without BRESHECK syndrome
GPathogenic
MBTPS2
(F475S)
Single nucleotide variant
(missense variant)
IFAP syndrome 1, with or without BRESHECK syndrome
GPathogenic
MBTPS2
(R429H)
Single nucleotide variant
(missense variant)
IFAP syndrome 1, with or without BRESHECK syndrome
+1 more
GPathogenic
MBTPS2
(M87I)
Single nucleotide variant
(missense variant)
IFAP syndrome 1, with or without BRESHECK syndrome
GPathogenic
MBTPS2
(H227L)
Single nucleotide variant
(missense variant)
IFAP syndrome 1, with or without BRESHECK syndrome
GPathogenic
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