Phenotype #0000106260

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00133513
Associated disease	LGMDR5;LGMD2C
Phenotype details	-
Diagnosis/Initial	severe autosomal recessive muscular dystrophy, North African type (SCARMD)
Inheritance	Unknown
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	WB reduced SGCA
Owner name	Marina Fanin
Database submission license	No license selected
Created by	Marina Fanin
Date created	2014-12-11 11:11:14 +01:00 (CET)
Date last edited	N/A

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