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AMMECR1 gene

Known as: AMME CHROMOSOME REGION GENE 1, AMMECR1, Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 
 
National Institutes of Health

Papers overview

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2017
2017
In this study, we report a family with X-linked recessive syndrome caused by mutated AMMECR1 and characterized by elliptocytosis… Expand
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2016
2016
Osmanli Devleti'nden modern cumhuriyete giden surecte, ust duzey yoneticilerin yetistirilmesi, uzerinde onemle durulan konulardan… Expand
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2015
2015
Devlet yasalarla belirlenen olculer cercevesinde mukelleflerden vergi tahsil etme yetkisine sahiptir. Vergi yukunun adil ve… Expand
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2007
2007
mme idarelerinin alacaklar›n›n kanunlarda yer verilen surelerde oden- mesi (tahsili) esast›r. Ancak odeme zorluuna duflen… Expand
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2004
2004
encodes an uncharacterizedprotein of 333 amino acids. The N-terminal region ofAMMECR1 (from residue 1 to 121) is rich in glycine… Expand
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2000
2000
The contiguous gene deletion syndrome AMME is characterized by Alport syndrome, midface hypoplasia, mental retardation and… Expand
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1984
1984
SummaryThe most spectacular aspect is the extremely rapid expansion of medical law. Even if there is a close connection between… Expand
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