All individuals with variants in gene TUFM

10 entries on 1 page. Showing entries 1 - 10.
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00003025 - PubMed: Neveling 2013 - - - - - - - - - ? PMR, myopathy, Leigh syndrome 2 1 Marcel Nelen
00037293 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00037294 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00037295 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00037296 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00050458 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, intrauterine growth retardation, global developmental delay, abnormal size of the palpebral fissures, prominent nose, short 4th metacarpal, clinodactyly of the 5th finger, cutaneous syndactyly of toes, aggressive behavior 1 1 Johan den Dunnen
00050683 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) M - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, abnormality of the outer ear, prominent metopic ridge, narrow mouth, inferior vermis hypoplasia, delayed speech and language development 1 2 Johan den Dunnen
00073552 - PubMed: Valente 2007 family, 1 affected, unaffected heterozygous carrier parents/sibs F no Italy Tyrol, south 01y02m - - - COXPD4 see paper; ..., died at 14m 1 1 Johan den Dunnen
00210166 - - - M - Germany - - - - - - HP:0004904 (Maturity-onset diabetes of the young) 1 1 Andreas Laner
00390025 3 PubMed: Ruberto 2020 - ? - Italy - - - - - retinal disease Pale and tilted optic disk associated to hypoplasia, tortuous retinal vessels, non-homogeneous macula 1 1 LOVD
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