Calpainopathy: how broad is the spectrum of clinical variability? (Q44674350)

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Language	Label	Description	Also known as
English	Calpainopathy: how broad is the spectrum of clinical variability?	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Calpainopathy: how broad is the spectrum of clinical variability? (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

5

object named as

Mayana Zatz

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Flavia de Paula

object named as

Flavia de Paula

2

0 references

object named as

Mariz Vainzof

4

0 references

author name string

Alessandra Starling

1

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Helga Silva

3

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

publication date

1 January 2003

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Journal of Molecular Neuroscience

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Europe PubMed Central

PubMed publication ID

5 December 2017

21

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

233-236

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Clinical variability in calpainopathy: what makes the difference?

1 reference

https://pubmed.ncbi.nlm.nih.gov/14645990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/14645990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14645990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Making sense of the limb-girdle muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/14645990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage

1 reference

https://pubmed.ncbi.nlm.nih.gov/14645990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 10 autosomal recessive limb-girdle muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/14645990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apparent autosomal recessive inheritance in families with proximal spinal muscular atrophy affecting individuals in two generations

1 reference

https://pubmed.ncbi.nlm.nih.gov/14645990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1385/JMN:21:3:233

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

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