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Carolyn Hart | Researcher profile | ResearchHub

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Carolyn Hart

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Researcher profile

Carolyn Hart

ResearchHub researcher

1

Publications

57

Citations

1

H-index

0

Recent H-index

2

Reads

0

Followers

Overview Research Publications Projects Datasets Questions Impact Network Activity

Overview

Research identity

Research areas

Not available

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Research

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Public works are drawn from admitted ResearchHub scholarly records.

Publications

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1 of 1 listed works

Exports contain available public metadata for the works currently shown.

Mutations in the δ-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)

Neurogenetics · 1997 · journal-article

57 citations · 2 reads

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Impact

Measured impact

Publications: 1
Citations: 57
H-index: 1
Recent H-index: 0
Reads: 2

H-index follows the standard Hirsch definition: the largest h for which h publications each have at least h citations. Recent H-index applies the same calculation to the five most recent complete calendar years (2021-2025); the current year is excluded while incomplete.

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Network

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0 followers

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Activity

Recent activity

Not available

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Not available