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Spastic paraplegia "11," autosomal recessive
- ... More About This Health Condition FLJ21439 KIAA1840 spastic paraplegia 11 (autosomal recessive) SPATACSIN SPTCS_HUMAN Tests of SPG11 PubMed SPG11 ...
- ... Organization for Rare Disorders (NORD) ClinicalTrials.gov SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11 PubMed Denora PS, Schlesinger D, Casali C, ...
- ... Hereditary spastic paraplegia Genetic Testing Registry: Hereditary spastic paraplegia 15 Autosomal recessive spastic paraplegia type 15 Hereditary spastic paraplegia National ...
- ... hydroxylase domain containing 1 FAXDC1 FLJ25287 SCS7 spastic paraplegia 35 (autosomal recessive) SPG35 Tests of FA2H PubMed FATTY ACID 2- ...
- ... Organization for Rare Disorders (NORD) ClinicalTrials.gov SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE, WITH OR WITHOUT NEURODEGENERATION; SPG35 PubMed Arber CE, ...
- ... encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. Am J Hum Genet. 2008 ...
- ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ... Genetic Testing Registry: Hereditary spastic paraplegia Genetic Testing ...
- ... In several families, Kallmann syndrome has shown an autosomal recessive pattern of inheritance. Autosomal recessive inheritance means both copies of the gene in ...
- ... adulthood. GRN CLN11 disease is inherited in an autosomal recessive pattern, which means both copies of the gene ...