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1
Q47973718-7C1FD5E0-5DC2-4B3E-8E77-3EAD9D9312B1
Q47973718-7C1FD5E0-5DC2-4B3E-8E77-3EAD9D9312B1
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Statement
http://www.wikidata.org/entity/statement/Q47973718-7C1FD5E0-5DC2-4B3E-8E77-3EAD9D9312B1
Clinical diversity caused by novel IGHMBP2 variants.
P2860
Q47973718-7C1FD5E0-5DC2-4B3E-8E77-3EAD9D9312B1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47973718-7C1FD5E0-5DC2-4B3E-8E77-3EAD9D9312B1
rank
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type
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Statement
wasDerivedFrom
ecf993be7f4e49150f1871508b887000c8496455
P2860
PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease.