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Q28181983-0A394AFB-A7AC-4612-84E8-0B94C6BDDFDA
Q28181983-0A394AFB-A7AC-4612-84E8-0B94C6BDDFDA
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http://www.wikidata.org/entity/statement/Q28181983-0A394AFB-A7AC-4612-84E8-0B94C6BDDFDA
Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases
P2860
Q28181983-0A394AFB-A7AC-4612-84E8-0B94C6BDDFDA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28181983-0A394AFB-A7AC-4612-84E8-0B94C6BDDFDA
rank
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type
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wasDerivedFrom
1f5712141d1429a6733c4f820d1cb22508b170ba
P2860
A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency