I-cell disease (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "I-cell disease" in English language version.

refsWebsite

Global rank English rank

3web.archive.org

1^st place

1^st place

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2^nd place

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4^th place

2semanticscholar.org

11^th place

8^th place

7,201^st place

low place

3,673^rd place

2,870^th place

1rarediseases.org

5,181^st place

3,260^th place

1,266^th place

860^th place

low place

low place

doi.org

Plante M, Claveau S, Lepage P, et al. (March 2008). "Mucolipidosis II: a single causal mutation in the N-acetylglucosamine-1-phosphotransferase gene (GNPTAB) in a French Canadian founder population" (PDF). Clin. Genet. 73 (3): 236–44. doi:10.1111/j.1399-0004.2007.00954.x. PMID 18190596. S2CID 20999105.
Tiede S, Storch S, Lübke T, et al. (2005). "Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase". Nat. Med. 11 (10): 1109–12. doi:10.1038/nm1305. PMID 16200072. S2CID 24959938.

gov.mt

sahha.gov.mt

"Sahha.gov.mt - 2006 Dec;29_1". Archived from the original on 2012-02-26. Retrieved 2009-09-16.

nih.gov

pubmed.ncbi.nlm.nih.gov

Plante M, Claveau S, Lepage P, et al. (March 2008). "Mucolipidosis II: a single causal mutation in the N-acetylglucosamine-1-phosphotransferase gene (GNPTAB) in a French Canadian founder population" (PDF). Clin. Genet. 73 (3): 236–44. doi:10.1111/j.1399-0004.2007.00954.x. PMID 18190596. S2CID 20999105.
Tiede S, Storch S, Lübke T, et al. (2005). "Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase". Nat. Med. 11 (10): 1109–12. doi:10.1038/nm1305. PMID 16200072. S2CID 24959938.

rarediseases.org

"I Cell Disease - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). Retrieved 2017-11-02.

semanticscholar.org

api.semanticscholar.org

Plante M, Claveau S, Lepage P, et al. (March 2008). "Mucolipidosis II: a single causal mutation in the N-acetylglucosamine-1-phosphotransferase gene (GNPTAB) in a French Canadian founder population" (PDF). Clin. Genet. 73 (3): 236–44. doi:10.1111/j.1399-0004.2007.00954.x. PMID 18190596. S2CID 20999105.
Tiede S, Storch S, Lübke T, et al. (2005). "Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase". Nat. Med. 11 (10): 1109–12. doi:10.1038/nm1305. PMID 16200072. S2CID 24959938.

umn.edu

bmt.umn.edu

"Inherited Metabolic Storage Diseases and BMT - MED - PEDS - Blood and Marrow Transplantation Program, University of Minnesota". Archived from the original on 2010-06-20. Retrieved 2009-12-01.

uqac.ca

constellation.uqac.ca

Plante M, Claveau S, Lepage P, et al. (March 2008). "Mucolipidosis II: a single causal mutation in the N-acetylglucosamine-1-phosphotransferase gene (GNPTAB) in a French Canadian founder population" (PDF). Clin. Genet. 73 (3): 236–44. doi:10.1111/j.1399-0004.2007.00954.x. PMID 18190596. S2CID 20999105.

web.archive.org

"mucolipidosis II" at Dorland's Medical Dictionary
"Sahha.gov.mt - 2006 Dec;29_1". Archived from the original on 2012-02-26. Retrieved 2009-09-16.
"Inherited Metabolic Storage Diseases and BMT - MED - PEDS - Blood and Marrow Transplantation Program, University of Minnesota". Archived from the original on 2010-06-20. Retrieved 2009-12-01.

ygf4icell.org

"Yash Gandhi Foundation". Yash Gandhi Foundation. Retrieved 2023-09-25.