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Q52684768-1E41C0C1-7BD4-4DCE-8E1B-6C0F268FB2CA
Q52684768-1E41C0C1-7BD4-4DCE-8E1B-6C0F268FB2CA
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http://www.wikidata.org/entity/statement/Q52684768-1E41C0C1-7BD4-4DCE-8E1B-6C0F268FB2CA
Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient series.
P2860
Q52684768-1E41C0C1-7BD4-4DCE-8E1B-6C0F268FB2CA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52684768-1E41C0C1-7BD4-4DCE-8E1B-6C0F268FB2CA
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wasDerivedFrom
43b804546d7bb454ab220f1b8b227dc0a4a849ce
P2860
CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes