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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

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
X-linked elliptocytosis with impaired growth is related to mutated AMMECR1.
2016
2016
TANZİMAT SONRASI DÖNEMDEN GÜNÜMÜZE ÜST DÜZEY YÖNETİCİ EĞITİMİ
Osmanli Devleti'nden modern cumhuriyete giden surecte, ust duzey yoneticilerin yetistirilmesi, uzerinde onemle durulan konulardan… 
2015
2015
Vergi Uyuşmazlıkları ve Vergi Yargılaması Usulü
Devlet yasalarla belirlenen olculer cercevesinde mukelleflerden vergi tahsil etme yetkisine sahiptir. Vergi yukunun adil ve… 
2007
2007
TEC‹L VE TAKS‹TLEND‹RME TEC‹L VE TAKS‹TLEND‹RME UYGULAMASI UYGULAMASI
mme idarelerinin alacaklar›n›n kanunlarda yer verilen surelerde oden- mesi (tahsili) esast›r. Ancak odeme zorluuna duflen… 
2005
2005
Die neuere Entwicklung des Arztrechts
SummaryThe most spectacular aspect is the extremely rapid expansion of medical law. Even if there is a close connection between… 
2004
2004
Crystal structure of PH0010 from Pyrococcus horikoshii, which is highly homologous to human AMMECR 1C‐terminal region
encodes an uncharacterizedprotein of 333 amino acids. The N-terminal region ofAMMECR1 (from residue 1 to 121) is rich in glycine… 
2000
2000
Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1–F3
The contiguous gene deletion syndrome AMME is characterized by Alport syndrome, midface hypoplasia, mental retardation and… 
1958
1958
MİLLETLERARASI AMME HİZMETİ MEFHUMU
1949
1949
Kronik: Amme Kanunlarının Verdiği Yetkinin Devri Meselesi
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