About: Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

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About: Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1 Goto Sponge NotDistinct Permalink

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description	article científic (ca) article scientific (oc) articol științific (ro) articolo scientifico (it) artigo científico (gl) artikull shkencor (sq) artikulong pang-agham (tl) artykuł naukowy (pl) bilimsel makale (tr) mokslinis straipsnis (lt) scienca artikolo (eo) teaduslik artikkel (et) tieteellinen artikkeli (fi) tudományos cikk (hu) vetenskaplig artikel (sv) vitenskapelig artikkel (nb) vitskapeleg artikkel (nn) wissenschaftlicher Artikel (de) επιστημονικό άρθρο (el) мақолаи илмӣ (tg) научна статия (bg) научная статья (ru) מאמר מדעי (he) სამეცნიერო სტატია (ka) บทความทางวิทยาศาสตร์ (th) bài báo khoa học (vi) naučni članak (sr-el) мақолаи илмӣ (tg-cyrl) научни чланак (sr-ec) scientific article (en) سائنسی مضمون (ur) مقالهٔ علمی (fa) 1993 nî lūn-bûn (nan) 1993年の論文 (ja) 1993年論文 (zh-hk) 1993年論文 (zh-tw) 1993年論文 (zh-hant) 1993年論文 (yue) 1993年論文 (zh-mo) 1993年论文 (zh) 1993年论文 (zh-cn) 1993年论文 (zh-sg) 1993年论文 (zh-hans) 1993年论文 (wuu) 1993年论文 (zh-my) 1993년 논문 (ko) article scientifique (publié 1993) (fr) artigo científico (publicado na 1993) (pt) artigo científico (publicado na 1993) (pt-br) artículo científico publicado en 1993 (es) artículu científicu espublizáu en 1993 (ast) vědecký článek publikovaný v roce 1993 (cs) ১৯৯৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ (bn) مقالة علمية (نشرت في يوليو 1993) (ar) 1993 թուականի Յուլիսին հրատարակուած գիտական յօդուած (hyw) vedecký článok (publikovaný 1993-07) (sk) 1993 թվականի հուլիսին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в липні 1993 (uk) научни чланак (објављен 1993-07) (sr) videnskabelig artikel (udgivet 1993) (da) wetenschappelijk artikel (gepubliceerd in 1993-07) (nl) 1993ജൂലൈ 1 നു പ്രസിദ്ധീകരിച്ച ശാസ്ത്ര ലേഖനം (ml)
publication date	wds:Q28261862-2B5FB5A9-F93F-4D2B-B876-74A1F3DBF316
publication date	1993-07-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28261862-7BC59C4A-60B7-4839-84FA-87F398DAF614
language of work or name	English
exact match	wds:Q28261862-9763D826-B089-4184-86DD-58B47D65E20D
exact match	https://scigraph.springernature.com/pub.10.1038/ng0793-295
cites work	wds:Q28261862-263BE3CF-1EEB-431A-BDB7-D861276F3329 wds:Q28261862-30BF6247-5FC3-4E87-B86C-D8FD19EC9246 wds:Q28261862-342B1DD4-4F85-442E-BA2A-EED19D9A716B wds:Q28261862-348C9E51-F29A-47C9-B337-046CD9DF7B1C wds:Q28261862-36419470-CCBC-4B9F-96AA-9D8CE5063E79 wds:Q28261862-3F24EB6B-EF83-4337-802A-79DC03B5F0DA wds:Q28261862-87427F91-A480-4D54-B3AC-592CA5D261D5 wds:Q28261862-9E969EF1-1CC5-4298-8C6F-E8343FA3C912 wds:Q28261862-AB4799F6-6924-42C8-8DC5-DC0D223C33DD wds:Q28261862-B14A8E88-FF28-45E2-B6DB-B6EC67D49950 wds:Q28261862-CAFE971D-B642-44C0-8020-EB463F636633 wds:Q28261862-CB44F94A-D523-4840-B2BF-50744017EA49 wds:Q28261862-D56A7702-70E7-4BED-B25A-E30D636BC272 wds:Q28261862-D79152B7-01C3-4E5B-85C9-D41C3595D564
cites work	Positional cloning: let's not call it reverse anymore Dominant spinopontine atrophy. Report of two additional members of family W Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba Dinucleotide repeat polymorphism at the D6S89 locus Dinucleotide repeat polymorphism at the D6S109 locus Strategies for multilocus linkage analysis in humans Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French families. Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990). The human gene encoding insulin-like growth factor I is located on chromosome 12. Azorean disease of the nervous system. Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through six generations. Search for the chromosomal location of autosomal dominant cerebellar ataxia from Holguin, Cuba: exclusion from candidate regions on chromosome 4 and 11q
author name string	wds:Q28261862-52123C15-821F-4429-B3D1-679A98E48EBF wds:Q28261862-60806177-193F-465C-9E31-94F143ABD47D wds:Q28261862-68C053F4-2D38-43D3-A688-F3E97E28B219

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