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Year | Number of Results |
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1993 | 1 |
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PubMed (cited) for id: 139080
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A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family.
Br J Dermatol. 2018 Feb;178(2):556-558. doi: 10.1111/bjd.15661. Epub 2017 Dec 1.
Br J Dermatol. 2018.
PMID: 28504827
Free PMC article.
No abstract available.
The yeast mitochondrial carrier Leu5p and its human homologue Graves' disease protein are required for accumulation of coenzyme A in the matrix.
Prohl C, Pelzer W, Diekert K, Kmita H, Bedekovics T, Kispal G, Lill R.
Prohl C, et al.
Mol Cell Biol. 2001 Feb;21(4):1089-97. doi: 10.1128/MCB.21.4.1089-1097.2001.
Mol Cell Biol. 2001.
PMID: 11158296
Free PMC article.
Item in Clipboard
Regional assignment of the gene coding for a human Graves' disease autoantigen to 10q21.3-q22.1.
Rossi E, Zarrilli R, Zuffardi O.
Rossi E, et al.
Hum Genet. 1993 Feb;90(6):653-4. doi: 10.1007/BF00202485.
Hum Genet. 1993.
PMID: 8444471
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Sequence and chromosomal assignment of a novel cDNA identified by immunoscreening of a thyroid expression library: similarity to a family of mitochondrial solute carrier proteins.
Zarrilli R, Oates EL, McBride OW, Lerman MI, Chan JY, Santisteban P, Ursini MV, Notkins AL, Kohn LD.
Zarrilli R, et al.
Mol Endocrinol. 1989 Sep;3(9):1498-505. doi: 10.1210/mend-3-9-1498.
Mol Endocrinol. 1989.
PMID: 2575220
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