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Ataxia - paediatric v0.241 LAMA1 Zornitza Stark Publications for gene: LAMA1 were set to 26932191
Ataxia - paediatric v0.240 LAMA1 Zornitza Stark commented on gene: LAMA1: Five unrelated families reported.
Ataxia - paediatric v0.240 LAMA1 Zornitza Stark edited their review of gene: LAMA1: Changed publications: 25105227
Ataxia - paediatric v0.197 LAMA1 Zornitza Stark Marked gene: LAMA1 as ready
Ataxia - paediatric v0.197 LAMA1 Zornitza Stark Gene: lama1 has been classified as Green List (High Evidence).
Ataxia - paediatric v0.0 LAMA1 Bryony Thompson gene: LAMA1 was added
gene: LAMA1 was added to Ataxia - paediatric_RMH. Sources: Expert Review Green,GeneReviews,Royal Melbourne Hospital
Mode of inheritance for gene: LAMA1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: LAMA1 were set to 26932191
Phenotypes for gene: LAMA1 were set to Poretti-Boltshauser syndrome; Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome