Literature DB >> 14902756

Hereditary ataxia; a survey of certain clinical, pathologic and genetic features with linkage data on five additional hereditary factors.

J W SCHUT.   

Abstract

Entities:  

Keywords:  HEREDITARY SPINAL SCLEROSIS/heredity

Mesh：

Year:  1951        PMID： 14902756      PMCID： PMC1716319     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  2 in total

1.  Estimation of linkage in Rucker's pedigree of nystagmus and colorblindness.

Authors:  H W Norton
Journal:  Am J Hum Genet       Date:  1949-09       Impact factor: 11.025

2.  A New Human Hereditary Blood Property (Cellano) Present in 99.8% of all Bloods.

Authors:  P Levine; M Backer; M Wigod; R Ponder
Journal:  Science       Date:  1949-05-06       Impact factor: 47.728
  2 in total
  2 in total

1.  Blood-group studies in Friedreich's ataxia.

Authors:  E D POWELL
Journal:  Br Med J       Date:  1961-03-25

Review 2.  A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature.

Authors:  Mohammad A Al-Muhaizea; Faten AlMutairi; Rawan Almass; Safinaz AlHarthi; Mazhor S Aldosary; Maysoon Alsagob; Ali AlOdaib; Dilek Colak; Namik Kaya
Journal:  Cerebellum       Date:  2018-06       Impact factor: 3.847
  2 in total

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