Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q (Q24672217): Difference between revisions

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Property / cites work
 
Property / cites work: HEREDITARY SPASTIC PARAPLEGIA. / rank
 
Normal rank
Property / cites work: HEREDITARY SPASTIC PARAPLEGIA. / reference
 
stated in: PubMed Central
reference URL: https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321
retrieved: 28 November 2018
Timestamp+2018-11-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / cites work
 
Property / cites work: Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene / rank
 
Normal rank
Property / cites work: Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene / reference
 
stated in: PubMed Central
reference URL: https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321
retrieved: 28 November 2018
Timestamp+2018-11-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / cites work
 
Property / cites work: Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia / rank
 
Normal rank
Property / cites work: Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia / reference
 
stated in: PubMed Central
reference URL: https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321
retrieved: 28 November 2018
Timestamp+2018-11-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Revision as of 18:05, 28 November 2018

scientific article
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English
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q
scientific article

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    Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q (English)
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    J K Fink
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    C T Wu
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    S M Jones
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    G B Sharp
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    B M Lange
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    A Lesicki
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    T Reinglass
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    T Varvil
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    B Otterud
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    M Leppert
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    January 1995
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    56
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    1
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    188-92
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