All individuals with variants in gene TRPM6

10 entries on 1 page. Showing entries 1 - 10.
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AscendingIndividual ID     

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VIP     

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Owner     
00016698 - PubMed: Schlingmann 2002 5-generation family, 2 affecteds (F1.1, F1.2), unaffected carriers F yes Turkey white - - - - HOMG1 initial Mg2+ 0.21 mM, FE Mg2+ 4.8%; age onset 9w 1 1 Karl Schlingmann
00016701 - PubMed: Schlingmann 2002 4-generation family, 1 affected, unaffected carrier parents M yes Turkey white - - - - HOMG1 initial Mg2+ 0.08 mM, FE Mg2+ 2.8%; age onset 3w 1 1 Karl Schlingmann
00016705 - PubMed: Schlingmann 2002 - F - Sweden white - - - - HOMG1 initial Mg2+ 0.10 mM, FE Mg2+ 4.0% 2 1 Karl Schlingmann
00016707 - PubMed: Schlingmann 2002 - ? no Israel Jewish - - - - HOMG1 initial Mg2+ 0.41 mM, FE Mg2+high; age onset 4w 2 1 Karl Schlingmann
00016708 - PubMed: Schlingmann 2002 4-generation family, 2 affected sisters (F5.1/F5.2), unaffected carrier parents F yes Albania white - - - - HOMG1 initial Mg2+ 0.17 mM, FE Mg2+ 4.5%; age onset 5w 1 1 Karl Schlingmann
00016843 - PubMed: Schlingmann 2002 4-generation family, 2 affected sisters (F5.1/F5.2), unaffected carrier parents F yes Albania - - - - - HOMG1 initial Mg2+ 0.22 mM, FE Mg2+ 2.6%; age onset 5w 1 1 Karl Schlingmann
00231400 John Sayer - - F yes Oman - 05y - - - HOMG1 hypomagnesemia (HP:0002917), hypocalcaemia (HP:0002901) 1 3 John Sayer
00294883 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00414236 201120 - - F likely Germany - - - - - HOMG1 Hypomagnesemia, Seizure 1 1 Andreas Laner
00427997 A089 PubMed: Bournazos 2022 family, 1 affected M - Australia - - - - - ? hypomagnesaemia, seizures, developmental delay 2 1 Johan den Dunnen
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