All individuals with variants in gene CLUAP1

4 entries on 1 page. Showing entries 1 - 4.
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00386928 Pat5 PubMed: Mauro-Herrera 2021 - - - United States - - - - - retinal disease - 2 1 Johan den Dunnen
00405903 - PubMed: Soens 2016 - - - - Saudi Arabian - - - - retinal disease severe visual function limited to light perception by 6 weeks of age, accompanied by nystagmus, the oculodigital sign, and an extinguished electroretinogram 1 1 LOVD
00405904 - PubMed: Johnston 2017 - - - (United States) - - - - - retinal disease Pallister–Hall syndrome; midline notched upper lip, alveolar ridge overgrowth, high palate, extra frenula, a malformed epiglottis with a midline cleft, and a notched tongue tip; His limb findings were remarkable for mild rhizomelic shortening, bilateral postaxial polydactyly with partial cutaneous syndactyly of fingers 4-5, bilateral preaxial polydactyly with partial cutaneous syndactyly of toes 2-3, broadened metatarsals, short fingers and toes, and small nails 1 1 LOVD
00405905 - PubMed: Johnston 2017 - - - (United States) - - - - - retinal disease Pallister–Hall syndrome; midline notched upper lip, alveolar ridge overgrowth, high palate, extra frenula, a malformed epiglottis with a midline cleft, and a notched tongue tip; His limb findings were remarkable for mild rhizomelic shortening, bilateral postaxial polydactyly with partial cutaneous syndactyly of fingers 4–5, bilateral preaxial polydactyly with partial cutaneous syndactyly of toes 2–3, broadened metatarsals, short fingers and toes, and small nails 1 1 LOVD
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