(Q35003187)

5 August 2017

title

2q37 as a susceptibility locus for idiopathic basal ganglia calcification (IBGC) in a large South Tyrolean family (English)

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basal ganglia calcification

5 August 2017

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8

Andrew Hicks

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5 August 2017

Claudia Béu Volpato

1

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5 August 2017

Alessandro De Grandi

2

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5 August 2017

Ebba Buffone

3

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5 August 2017

Maurizio Facheris

4

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5 August 2017

Uwe Gebert

5

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5 August 2017

Günther Schifferle

6

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5 August 2017

Rudolf Schönhuber

7

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5 August 2017

Peter P Pramstaller

9

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5 August 2017

publication date

1 November 2009

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Journal of Molecular Neuroscience

5 August 2017

published in

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5 August 2017

volume

39

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5 August 2017

issue

3

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5 August 2017

page(s)

346-353

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https://scigraph.springernature.com/pub.10.1007/s12031-009-9287-3

5 August 2017

exact match

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cites work

Familial idiopathic striopallidodentate calcifications

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https://api.crossref.org/works/10.1007%2FS12031-009-9287-3

Experimental tests of the adaptive significance of sexual recombination

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12031-009-9287-3

Neuropsychological alterations in patients with computed tomography-detected basal ganglia calcification

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12031-009-9287-3

Linkage studies in familial idiopathic basal ganglia calcification: separating the wheat from the chaff

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12031-009-9287-3

Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-009-9287-3

Exclusion of linkage to chromosome 14q in a large South Tyrolean family with Idiopathic Basal Ganglia Calcification (IBGC).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-009-9287-3

Heredofamilial brain calcinosis syndrome

21 January 2018

1 reference

12 December 2020

Japanese family with an autosomal dominant chromosome instability syndrome: a new neurodegenerative disease?

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12 December 2020

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

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12 December 2020

Biochemical characterization of the serum fetuin-mineral complex

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12 December 2020

A single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab mice

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12 December 2020

Biotin-responsive basal ganglia disease: a novel entity

1 reference

12 December 2020

Molecular characterization of mitocalcin, a novel mitochondrial Ca2+-binding protein with EF-hand and coiled-coil domains

1 reference

12 December 2020

Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q.

1 reference

12 December 2020

Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease).

1 reference

12 December 2020

Familial calcification of the basal ganglions: a metabolic and genetic study.

1 reference

12 December 2020

Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease")

1 reference

12 December 2020

A high-resolution recombination map of the human genome

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12 December 2020

Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3

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12 December 2020

The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives

1 reference

12 December 2020

10.1007/S12031-009-9287-3

Identifiers

DOI

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5 August 2017

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