All individuals with variants in gene PTRH2

3 entries on 1 page. Showing entries 1 - 3.
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00225703 25558065-Fam13DG0215 PubMed: Alazami 2015, Journal: Alazami 2015 6-generation family, 2 affected brothers, unaffected heterozygous carrier parents/relatives M yes Saudi Arabia - - - - - ? see paper; …, global developmental delay, hearing loss, and ataxia 1 2 Johan den Dunnen
00361568 12DG1210 PubMed: Anazi 2017 familial M - Saudi Arabia - - - - - ID not syndromic; global developmental delay 1 1 Johan den Dunnen
00448517 287210 - - F yes Syria Kurdish - - - - IMNEPD Secondary microcephaly, Progressive gait ataxia, Abnormal foot morphology, Intellectual disability, Sensorineural hearing impairment, Neurodevelopmental delay 1 1 Andreas Laner
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