handedness < haploinsufficiency < haplotype | Facettes : |
List of bibliographic references indexed by haploinsufficiency
Number of relevant bibliographic references: 2.Ident. | Authors (with country if any) | Title |
---|---|---|
000B40 (2009) | Eng-King Tan [Singapour] ; F. Shaffra Refai [Singapour] ; Mobin Siddique [Singapour] ; Karen Yap [Singapour] ; Patrick Ho [Singapour] ; Stephanie Fook-Chong [Singapour] ; Yi Zhao [Singapour] | Clinically reported heterozygous mutations in the PINK1 kinase domain exert a gene dosage effect |
001921 (2002) | Andrew West [États-Unis] ; Magali Periquet [France] ; Sarah Lincoln [États-Unis] ; Christoph B. Lücking [France, Allemagne] ; David Nicholl [Royaume-Uni] ; Vincenzo Bonifati ; Nina Rawal [France] ; Thomas Gasser [Allemagne] ; Ebba Lohmann [France] ; Jean-François Deleuze [France] ; Demetrius Maraganore [États-Unis] ; Allan Levey [Géorgie (pays)] ; Nick Wood [Royaume-Uni] ; Alexandra Dürr [France] ; John Hardy [États-Unis] ; Alexis Brice [France] ; Matt Farrer [États-Unis] | Complex relationship between Parkin mutations and Parkinson disease |
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/ParkinsonV1/Data/Main/Exploration
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/KwdEn.i -k "haploinsufficiency"
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/KwdEn.i \ -Sk "haploinsufficiency" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= ParkinsonV1 |flux= Main |étape= Exploration |type= indexItem |index= KwdEn.i |clé= haploinsufficiency }}
This area was generated with Dilib version V0.6.23. |