Sökning: WFRF:(Holmgren Per) > Identification of a...
Fältnamn | Indikatorer | Metadata |
---|---|---|
000 | 03935naa a2200421 4500 | |
001 | oai:DiVA.org:liu-48709 | |
003 | SwePub | |
008 | 091011s2002 | |||||||||||000 ||eng| | |
009 | oai:DiVA.org:umu-5099 | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-487092 URI |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-50992 URI |
024 | 7 | a https://doi.org/10.1212/01.WNL.0000036617.04943.962 DOI |
040 | a (SwePub)liud (SwePub)umu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Carlsson, Annau Umeå universitet,Umeå centrum för molekylär medicin (UCMM)4 aut0 (Swepub:umu)canana03 |
245 | 1 0 | a Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1 |
264 | 1 | b Lippincott Williams & Wilkins,c 2002 |
338 | a print2 rdacarrier | |
520 | a Migraine is the most common type of chronic episodic headache. To find novel susceptibility genes for familial migraine with and without aura, a genomewide screen was performed in a large family from northern Sweden. Evidence of linkage was obtained on chromosome 6p12.2-p21.1, with a maximum two-point lod score of 5.41 for marker D6S452. The patients with migraine shared a common haplotype of 10 Mb between markers D6S1650 and D6S1960. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Neurologi0 (SwePub)302072 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Neurology0 (SwePub)302072 hsv//eng |
653 | a MEDICINE | |
653 | a MEDICIN | |
700 | 1 | a Forsgren, Larsu Umeå universitet,Klinisk neurovetenskap,Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden4 aut0 (Swepub:umu)lafo0001 |
700 | 1 | a Nylander, Per-Olofu Linköpings universitet,Hälsouniversitetet,Psykiatri4 aut0 (Swepub:liu)perny42 |
700 | 1 | a Hellman, Urban,d 1966-u Umeå universitet,Medicinsk och klinisk genetik,Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden4 aut0 (Swepub:umu)urhe0001 |
700 | 1 | a Forsman-Semb, Ku Umeå universitet,Medicinsk och klinisk genetik,Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden4 aut |
700 | 1 | a Holmgren, Gu Umeå universitet,Medicinsk och klinisk genetik,Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden4 aut |
700 | 1 | a Holmberg, Danu Umeå universitet,Umeå centrum för molekylär medicin (UCMM),Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden4 aut0 (Swepub:umu)daho0001 |
700 | 1 | a Holmberg, Mu Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)4 aut |
710 | 2 | a Umeå universitetb Umeå centrum för molekylär medicin (UCMM)4 org |
773 | 0 | t Neurologyd : Lippincott Williams & Wilkinsg 59:11, s. 1804-1807q 59:11<1804-1807x 0028-3878x 1526-632X |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-48709 |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-5099 |
856 | 4 8 | u https://doi.org/10.1212/01.WNL.0000036617.04943.96 |
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