Enfermedad de los ganglios basales sensible a la biotina (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Enfermedad de los ganglios basales sensible a la biotina" in Spanish language version.

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1guiametabolica.org

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guiametabolica.org

Defecto del transportador de tiamina tipo 2. Hospital Sant Joan de Déu, Barcelona. Unidad de enfermedades metabólicas hereditarias.

nih.gov

ncbi.nlm.nih.gov

Tabarki, Brahim; Al-Hashem, Amal; Alfadhel, Majid (1993). Adam, Margaret P., ed. Biotin-Thiamine-Responsive Basal Ganglia Disease. University of Washington, Seattle. Consultado el 24 de febrero de 2024.
GeneRewiews: Biotin-Thiamine-Responsive Basal Ganglia Disease. Consultado el 14 de enero de 2016
WQ, Al-Yamani E, Acierno JS, Slaugenhaupt S, Gillis T, MacDonald ME, Ozand PT, Gusella JF. Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3. Am J Hum Genet. 2005;77:16–26.

ghr.nlm.nih.gov

Genetics Home Reference: Biotin-thiamine-responsive basal ganglia disease. Consultado el 14 de enero de 2016.
Genetics Home Reference: SLC19A3. Consultado el 14 de enero de 2016

ojrd.com

VV.AA: Biotin-responsive basal ganglia disease should be renamed biotin-thiamine-responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of 18 new cases. Orphanet Journal of Rare Diseases, Vol 8, 2013.

omim.org

OMIM: Thiamine metabolism dysfuntion syndrome 2. Consultado el 14 de enero de 2016

orpha.net

Orphanet: Enfermedad de los ganglios basales sensible a la biotina. Consultado el 14 de enero de 2016