All individuals with variants in gene RTN2

4 entries on 1 page. Showing entries 1 - 4.
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00003012 Pat4mov;Pat11 PubMed: Neveling 2013, PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - M - - - - - - - SPG12 hereditary spastic paraplegia 1 1 Marcel Nelen
00292158 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 35 Mohammed Faruq
00304667 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00473005 Fam144Pat102 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M no Iran - - - - - ataxia Ataxia; Lower limbs neuropathy extended to upper limbs; Distal Upper & lower limbs neuropathy & muscle weakness; Mild pes cavus; Dysarthria; Brain MRI: T2 hyperintense signal change in dentate nuclei; Mild SNHL in Rt. ear revealed in audiogram; Mild diastolic dysfunction in Echocardiogram. 1 1 Johan den Dunnen
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