All individuals with variants in gene ATP2B2

6 entries on 1 page. Showing entries 1 - 6.
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00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 8 1 Yu Sun
00282311 - PubMed: Ficarella 2007 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00311384 Pat2 PubMed: Granadillo 2020 2-generation family, 1 affected, unaffected non-carrier parents M - China - - - - - NDD birth weight normal, length normal; normal height, normal weight, OFC -1.58; developmental delay/intellectual disability; no gross motor delay, no fine motor delay; speech delay; autism, attention deficit hyperactivity disorder; no hypotonia; no sleep problems; no hearing loss; normal vision; no musculoskeletal anomalies; triangular face, normal forehead, normal eyes, normal ears, normal nose, micrognathia; no gastrointestinal problems; no family history 1 1 Johan den Dunnen
00453308 OCD018901 PubMed: Cappi 2016 analysis 20 sporadic obsessive-compulsive disorder cases - - Brazil - - - - - ? - 1 1 Johan den Dunnen
00466362 - Pending - F - France - - - - - DFNB12 Myopathy Axial muscle weakness Muscle weakness Proximal muscle weakness Joint hypermobility Congenital sensorineural hearing impairment 1 1 Camille Verebi
00466411 - Pending - F - France - - - - - DFNB12 Myopathy * Axial muscle weakness * Muscle weakness * Proximal muscle weakness * Joint hypermobility * Congenital sensorineural hearing impairment 1 1 Camille Verebi
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