All individuals with variants in gene ESRRG

8 entries on 1 page. Showing entries 1 - 8.
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00390427 G001037 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - retinal disease - 1 1 LOVD
00466602 - Tutakhel, NVHG2025 T03 2-generation family, 1 affected, unaffected non-carrier parents M - Netherlands - - - - - ? see paper; ..., motor developmental delay, muscular hypotonia, ataxia, eye movement disorder 1 1 Johan den Dunnen
00466603 - Tutakhel, NVHG2025 T03 2-generation family, 1 affected, unaffected non-carrier parents M - - - - - - - ? see paper; ..., motor developmental delay, muscular hypotonia, ataxia, eye movement disorder 1 1 Johan den Dunnen
00466604 - Tutakhel, NVHG2025 T03 2-generation family, 1 affected, unaffected non-carrier parents F - - - - - - - ? see paper; ..., motor developmental delay, muscular hypotonia, ataxia, eye movement disorder 1 1 Johan den Dunnen
00466605 - Tutakhel, NVHG2025 T03 2-generation family, 1 affected, unaffected non-carrier parents F - - - - - - - ? see paper; ..., motor developmental delay, muscular hypotonia, ataxia, eye movement disorder 1 1 Johan den Dunnen
00466606 - Tutakhel, NVHG2025 T03 2-generation family, 1 affected, unaffected non-carrier parents F - - - - - - - ? see paper; ..., motor developmental delay, muscular hypotonia, ataxia, eye movement disorder 1 1 Johan den Dunnen
00466607 - Tutakhel, NVHG2025 T03 2-generation family, affected father/son M - - - - - - - ? see paper; ..., motor developmental delay, muscular hypotonia, ataxia, eye movement disorder 1 2 Johan den Dunnen
00466608 - Tutakhel, NVHG2025 T03 2-generation family, 1 affected, unaffected non-carrier parents F - - - - - - - ? see paper; ..., motor developmental delay, muscular hypotonia, ataxia, eye movement disorder 1 1 Johan den Dunnen
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