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Q35854171-1E7223AA-C61D-4F95-9F97-D4E0C126A0F8
Q35854171-1E7223AA-C61D-4F95-9F97-D4E0C126A0F8
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http://www.wikidata.org/entity/statement/Q35854171-1E7223AA-C61D-4F95-9F97-D4E0C126A0F8
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China.
P2860
Q35854171-1E7223AA-C61D-4F95-9F97-D4E0C126A0F8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35854171-1E7223AA-C61D-4F95-9F97-D4E0C126A0F8
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wasDerivedFrom
eff70b98fb1bcabe4b6f4e6785f1021aaf470f71
P2860
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.