All individuals with variants in gene NIPA1

7 entries on 1 page. Showing entries 1 - 7.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00183455 Patient XVII PubMed: Giugliano 2018 - M - Italy - - - - - MYOP onset congenital, congenital arthrogryposis, no muscle weakness, normal elevated CPK (1x), biopsy fiber type dystroportion 1 1 Teresa Giugliano
00210191 - - - M - Germany - - - - - - HP:0002493 (Upper motor neuron dysfunction); HP:0001258 (Spastic paraplegia) 1 1 Andreas Laner
00291161 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00300198 - - - F - - - - - - - ? Abnormality of the nervous system (HP:0000707) 1 1 Andreas Laner
00304458 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00476149 JC195 PubMed: Beecroft 2020 analysis 2249 neurology patients M - (Australia);(New Zealand) - - - - - SPG details not specified; ncorrelation clinical diagnosis with genetic diagnosis 1 1 Johan den Dunnen
00476150 MS196 PubMed: Beecroft 2020 analysis 2249 neurology patients M - (Australia);(New Zealand) - - - - - SPG details not specified; ncorrelation clinical diagnosis with genetic diagnosis 1 1 Johan den Dunnen
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