All individuals with variants in gene HTRA1

9 entries on 1 page. Showing entries 1 - 9.
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00050476 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) F - United Kingdom (Great Britain) - - - Decipher - ? clinodactyly of the 5th finger, specific learning disability, joint hypermobility, lumbar hyperlordosis, gingival overgrowth 1 2 Johan den Dunnen
00374757 S-2554 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00390466 Y014715 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - BSVD - 1 1 LOVD
00390467 Y015921 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - BSVD - 1 1 LOVD
00410565 Pat27 PubMed: Schuermans 2022 analysis 329 adult patients suffering from undiagnosed rare disease F - Belgium - - - - - ? see paper; ..., onset adulthood, cerebral white matter lesions, family history 1 1 Johan den Dunnen
00410568 Pat30 PubMed: Schuermans 2022 analysis 329 adult patients suffering from undiagnosed rare disease M - Belgium - - - - - ? see paper; ..., onset adulthood, recurrent stroke, cerebral white matter lesions, family history 1 1 Johan den Dunnen
00410578 Pat40 PubMed: Schuermans 2022 analysis 329 adult patients suffering from undiagnosed rare disease M - Belgium - - - - - ? see paper; ..., onset adulthood, cerebral white matter lesions, hearing loss, family history 1 1 Johan den Dunnen
00451163 071764 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - - - - - - - - - macular dystrophy - 1 1 Johan den Dunnen
00451666 296354 - - F - Germany - - - - - CADASIL2 Abnormal cerebral vascular morphology, Abnormal cerebral white matter morphology, Abnormal exteroceptive sensation 1 1 Andreas Laner
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