BabelNet

bn:05504712n

Noun Named Entity

No term available

Autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding fukutin (FKTN) on chromosome 9q31 Wikidata

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Sources

IS A

σπάνια πάθηση

GENETIC ASSOCIATION

fukutin

HEALTH SPECIALTY

νευρολογία