All individuals with variants in gene TSFM

4 entries on 1 page. Showing entries 1 - 4.
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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     
00000014 - PubMed: Bell 2011 - - - - - - 0 - - autism, BMD/DMD - 1 1 LOVD-team, but with Curator vacancy
00037288 - - - - - Germany - - 0 - - ? suspected mitochondriopathy (affected child), defect of respiratory chain complex I and IV , parents consanguine 1 1 Andreas Laner
00063251 - - - M - Spain - - 0 - - COXPD-3 - 1 1 NeuroMeGen
00064766 - PubMed: Neubauer 2017 Journal: Neubauer 2017 - M ? Switzerland European 00y04m 0 - - SIDS SIDS 1 1 Cordula Haas
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