Disentangling the roots of inherited hair disorders.

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description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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2008年學術文章

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name

Disentangling the roots of inherited hair disorders.

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Disentangling the roots of inherited hair disorders.

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type

Item

label

Disentangling the roots of inherited hair disorders.

@en

Disentangling the roots of inherited hair disorders.

@nl

prefLabel

Disentangling the roots of inherited hair disorders.

@en

Disentangling the roots of inherited hair disorders.

@nl

P1476

Disentangling the roots of inherited hair disorders.

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P2093

Eli Sprecher

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P2860

Alopecia universalis associated with a mutation in the human hairless gene

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

More than one gene involved in monilethrix: intracellular but also extracellular players

Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH

Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia

The molecular genetics of keratin disorders.

Determination of hair structure and shape.

Genetic diseases of junctions.

Identification of 6H1 as a P2Y purinoceptor: P2Y5.

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin.

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265-266

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10.1038/NG0308-265

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English

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2008-03-01T00:00:00Z

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5547953

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1010969988

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