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ADGRV1 gene

Known as: KIAA0686, G PROTEIN-COUPLED RECEPTOR 98, MONOGENIC AUDIOGENIC SEIZURE SUSCEPTIBILITY 1, MOUSE, HOMOLOG OF 
 
National Institutes of Health

Papers overview

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2016
2016
Distinguishing patients with monogenic diabetes from those with type 1 diabetes (T1D) is important for correct diagnosis… Expand
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Highly Cited
2014
Highly Cited
2014
Can genetic and clinical findings made in a single patient be considered sufficient to establish a causal relationship between… Expand
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Highly Cited
2014
Highly Cited
2014
We report the design of a targeted resequencing panel for monogenic dyslipidemias, LipidSeq, for the purpose of replacing Sanger… Expand
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2013
2013
Single crystals of novel orthorhombic (space group Pnnm) iron tetraboride FeB4 were synthesized at pressures above 8 GPa and high… Expand
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Review
2009
Review
2009
Susceptibility to the growing global public health problem of cardiovascular disease is associated with levels of plasma lipids… Expand
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Highly Cited
2006
Highly Cited
2006
Mutations in the DFNB31 gene encoding the PDZ scaffold protein whirlin are causative for hearing loss in man and mouse. Whirlin… Expand
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Highly Cited
2005
Highly Cited
2005
Usher syndrome (USH) is the most frequent cause of combined deaf-blindness in man. USH is clinically and genetically… Expand
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2004
2004
At approximately 6300 amino acids, very large G-protein-coupled receptor-1 (VLGR1, also termed Mass1) is the largest known cell… Expand
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Highly Cited
2004
Highly Cited
2004
Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes… Expand
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2000
2000
Febrile seizures (FSs) represent the most common form of childhood seizure. In the Japanese population, the incidence rate is as… Expand
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