All individuals with variants in gene PKHD1L1

4 entries on 1 page. Showing entries 1 - 4.
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00050326 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00443406 Fam1 PubMed: Redfield 2023, Journal: Redfield 2023 2-generation family, 1 affected, unaffected heterozygous parents F no United States - - - - - HL see paper; ..., slowly progressive mild to moderate bilateral sensorineural hearing loss 2 1 Johan den Dunnen
00443407 Fam2 PubMed: Redfield 2023, Journal: Redfield 2023 2-generation family, 1 affected, unaffected heterozygous parents M yes United States - - - - - HL see paper; ..., moderate to severe congenital bilateral sensorineural hearing loss 1 1 Johan den Dunnen
00443408 Fam3 PubMed: Redfield 2023, Journal: Redfield 2023 2-generation family, 1 affected M yes Korea - - - - - HL see paper; ..., severe congenital bilateral sensorineural hearing loss 1 1 Johan den Dunnen
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